Canonical Allele Identifier: CA343772193

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873074T>A (hg19) ; chr1:g.173903936T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903936T>A , CM000663.2:g.173903936T>A	GRCh38
NC_000001.10:g.173873074T>A , CM000663.1:g.173873074T>A	GRCh37
NC_000001.9:g.172139697T>A	NCBI36
NG_012462.1:g.18443A>T , LRG_577:g.18443A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1348A>T MANE Select	ENSP00000356671.3:p.Asn450Tyr
ENST00000367698.3:c.1348A>T	ENSP00000356671.3:p.Asn450Tyr
ENST00000617423.4:c.733A>T	ENSP00000478688.1:p.Asn245Tyr
NM_000488.3:c.1348A>T , LRG_577t1:c.1348A>T	NP_000479.1:p.Asn450Tyr
XM_005245198.2:c.1204A>T	XP_005245255.1:p.Asn402Tyr
NM_001365052.1:c.1204A>T	NP_001351981.1:p.Asn402Tyr
NM_000488.4:c.1348A>T MANE Select	NP_000479.1:p.Asn450Tyr
NM_001365052.2:c.1204A>T	NP_001351981.1:p.Asn402Tyr
NM_001386302.1:c.1471A>T	NP_001373231.1:p.Asn491Tyr
NM_001386303.1:c.1429A>T	NP_001373232.1:p.Asn477Tyr
NM_001386304.1:c.1327A>T	NP_001373233.1:p.Asn443Tyr
NM_001386305.1:c.1291A>T	NP_001373234.1:p.Asn431Tyr
NM_001386306.1:c.1132A>T	NP_001373235.1:p.Asn378Tyr