Canonical Allele Identifier: CA421821179
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173873039A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903901A>T , CM000663.2:g.173903901A>T GRCh38
NC_000001.10:g.173873039A>T , CM000663.1:g.173873039A>T GRCh37
NC_000001.9:g.172139662A>T NCBI36
NG_012462.1:g.18478T>A , LRG_577:g.18478T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.1383T>A MANE Select ENSP00000356671.3:p.Pro461=
ENST00000367698.3:c.1383T>A ENSP00000356671.3:p.Pro461=
ENST00000617423.4:c.768T>A ENSP00000478688.1:p.Pro256=
NM_000488.3:c.1383T>A , LRG_577t1:c.1383T>A NP_000479.1:p.Pro461=
XM_005245198.2:c.1239T>A XP_005245255.1:p.Pro413=
NM_001365052.1:c.1239T>A NP_001351981.1:p.Pro413=
NM_000488.4:c.1383T>A MANE Select NP_000479.1:p.Pro461=
NM_001365052.2:c.1239T>A NP_001351981.1:p.Pro413=
NM_001386302.1:c.1506T>A NP_001373231.1:p.Pro502=
NM_001386303.1:c.1464T>A NP_001373232.1:p.Pro488=
NM_001386304.1:c.1362T>A NP_001373233.1:p.Pro454=
NM_001386305.1:c.1326T>A NP_001373234.1:p.Pro442=
NM_001386306.1:c.1167T>A NP_001373235.1:p.Pro389=