Canonical Allele Identifier: CA343774229
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878917T>G (hg19) chr1:g.173909779T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909779T>G , CM000663.2:g.173909779T>G GRCh38
NC_000001.10:g.173878917T>G , CM000663.1:g.173878917T>G GRCh37
NC_000001.9:g.172145540T>G NCBI36
NG_012462.1:g.12600A>C , LRG_577:g.12600A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.926A>C MANE Select ENSP00000356671.3:p.Asp309Ala
ENST00000367698.3:c.926A>C ENSP00000356671.3:p.Asp309Ala
ENST00000487183.1:n.577A>C
ENST00000617423.4:c.559+2085A>C ENSP00000478688.1:n.559+2085A>C
NM_000488.3:c.926A>C , LRG_577t1:c.926A>C NP_000479.1:p.Asp309Ala
XM_005245198.2:c.782A>C XP_005245255.1:p.Asp261Ala
NM_001365052.1:c.782A>C NP_001351981.1:p.Asp261Ala
NM_000488.4:c.926A>C MANE Select NP_000479.1:p.Asp309Ala
NM_001365052.2:c.782A>C NP_001351981.1:p.Asp261Ala
NM_001386302.1:c.1049A>C NP_001373231.1:p.Asp350Ala
NM_001386303.1:c.1007A>C NP_001373232.1:p.Asp336Ala
NM_001386304.1:c.905A>C NP_001373233.1:p.Asp302Ala
NM_001386305.1:c.869A>C NP_001373234.1:p.Asp290Ala
NM_001386306.1:c.710A>C NP_001373235.1:p.Asp237Ala
Search 100 bp 5'
Search 100 bp 3'