Canonical Allele Identifier: CA343773741
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878803A>G (hg19) chr1:g.173909665A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909665A>G , CM000663.2:g.173909665A>G GRCh38
NC_000001.10:g.173878803A>G , CM000663.1:g.173878803A>G GRCh37
NC_000001.9:g.172145426A>G NCBI36
NG_012462.1:g.12714T>C , LRG_577:g.12714T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1040T>C MANE Select ENSP00000356671.3:p.Met347Thr
ENST00000367698.3:c.1040T>C ENSP00000356671.3:p.Met347Thr
ENST00000617423.4:c.560-2172T>C ENSP00000478688.1:n.560-2172T>C
NM_000488.3:c.1040T>C , LRG_577t1:c.1040T>C NP_000479.1:p.Met347Thr
XM_005245198.2:c.896T>C XP_005245255.1:p.Met299Thr
NM_001365052.1:c.896T>C NP_001351981.1:p.Met299Thr
NM_000488.4:c.1040T>C MANE Select NP_000479.1:p.Met347Thr
NM_001365052.2:c.896T>C NP_001351981.1:p.Met299Thr
NM_001386302.1:c.1163T>C NP_001373231.1:p.Met388Thr
NM_001386303.1:c.1121T>C NP_001373232.1:p.Met374Thr
NM_001386304.1:c.1019T>C NP_001373233.1:p.Met340Thr
NM_001386305.1:c.983T>C NP_001373234.1:p.Met328Thr
NM_001386306.1:c.824T>C NP_001373235.1:p.Met275Thr
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