Canonical Allele Identifier: CA343774323
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909803A>G , CM000663.2:g.173909803A>G GRCh38
NC_000001.10:g.173878941A>G , CM000663.1:g.173878941A>G GRCh37
NC_000001.9:g.172145564A>G NCBI36
NG_012462.1:g.12576T>C , LRG_577:g.12576T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.902T>C MANE Select ENSP00000356671.3:p.Val301Ala
ENST00000367698.3:c.902T>C ENSP00000356671.3:p.Val301Ala
ENST00000487183.1:n.553T>C
ENST00000617423.4:c.559+2061T>C ENSP00000478688.1:n.559+2061T>C
NM_000488.3:c.902T>C , LRG_577t1:c.902T>C NP_000479.1:p.Val301Ala
XM_005245198.2:c.758T>C XP_005245255.1:p.Val253Ala
NM_001365052.1:c.758T>C NP_001351981.1:p.Val253Ala
NM_000488.4:c.902T>C MANE Select NP_000479.1:p.Val301Ala
NM_001365052.2:c.758T>C NP_001351981.1:p.Val253Ala
NM_001386302.1:c.1025T>C NP_001373231.1:p.Val342Ala
NM_001386303.1:c.983T>C NP_001373232.1:p.Val328Ala
NM_001386304.1:c.881T>C NP_001373233.1:p.Val294Ala
NM_001386305.1:c.845T>C NP_001373234.1:p.Val282Ala
NM_001386306.1:c.686T>C NP_001373235.1:p.Val229Ala