Canonical Allele Identifier: CA343773687
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909652G>C , CM000663.2:g.173909652G>C GRCh38
NC_000001.10:g.173878790G>C , CM000663.1:g.173878790G>C GRCh37
NC_000001.9:g.172145413G>C NCBI36
NG_012462.1:g.12727C>G , LRG_577:g.12727C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1053C>G MANE Select ENSP00000356671.3:p.His351Gln
ENST00000367698.3:c.1053C>G ENSP00000356671.3:p.His351Gln
ENST00000617423.4:c.560-2159C>G ENSP00000478688.1:n.560-2159C>G
NM_000488.3:c.1053C>G , LRG_577t1:c.1053C>G NP_000479.1:p.His351Gln
XM_005245198.2:c.909C>G XP_005245255.1:p.His303Gln
NM_001365052.1:c.909C>G NP_001351981.1:p.His303Gln
NM_000488.4:c.1053C>G MANE Select NP_000479.1:p.His351Gln
NM_001365052.2:c.909C>G NP_001351981.1:p.His303Gln
NM_001386302.1:c.1176C>G NP_001373231.1:p.His392Gln
NM_001386303.1:c.1134C>G NP_001373232.1:p.His378Gln
NM_001386304.1:c.1032C>G NP_001373233.1:p.His344Gln
NM_001386305.1:c.996C>G NP_001373234.1:p.His332Gln
NM_001386306.1:c.837C>G NP_001373235.1:p.His279Gln