Canonical Allele Identifier: CA343774693
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909890T>G , CM000663.2:g.173909890T>G GRCh38
NC_000001.10:g.173879028T>G , CM000663.1:g.173879028T>G GRCh37
NC_000001.9:g.172145651T>G NCBI36
NG_012462.1:g.12489A>C , LRG_577:g.12489A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.815A>C MANE Select ENSP00000356671.3:p.Tyr272Ser
ENST00000367698.3:c.815A>C ENSP00000356671.3:p.Tyr272Ser
ENST00000487183.1:n.466A>C
ENST00000617423.4:c.559+1974A>C ENSP00000478688.1:n.559+1974A>C
NM_000488.3:c.815A>C , LRG_577t1:c.815A>C NP_000479.1:p.Tyr272Ser
XM_005245198.2:c.671A>C XP_005245255.1:p.Tyr224Ser
NM_001365052.1:c.671A>C NP_001351981.1:p.Tyr224Ser
NM_000488.4:c.815A>C MANE Select NP_000479.1:p.Tyr272Ser
NM_001365052.2:c.671A>C NP_001351981.1:p.Tyr224Ser
NM_001386302.1:c.938A>C NP_001373231.1:p.Tyr313Ser
NM_001386303.1:c.896A>C NP_001373232.1:p.Tyr299Ser
NM_001386304.1:c.794A>C NP_001373233.1:p.Tyr265Ser
NM_001386305.1:c.763-5A>C NP_001373234.1:n.763-5A>C
NM_001386306.1:c.599A>C NP_001373235.1:p.Tyr200Ser