Canonical Allele Identifier: CA32782275

Gene: SERPINC1

Linked Data

• dbSNP Id: rs199469507

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173914725_173914732delinsTCCC , CM000663.2:g.173914725_173914732delinsTCCC	GRCh38
NC_000001.10:g.173883863_173883870delinsTCCC , CM000663.1:g.173883863_173883870delinsTCCC	GRCh37
NC_000001.9:g.172150486_172150493delinsTCCC	NCBI36
NG_012462.1:g.7647_7654delinsGGGA , LRG_577:g.7647_7654delinsGGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.229_236delinsGGGA MANE Select	ENSP00000356671.3:p.Asn77GlyfsTer?
ENST00000367698.3:c.229_236delinsGGGA	ENSP00000356671.3:p.Asn77GlyfsTer?
ENST00000494024.1:n.455_462delinsGGGA
ENST00000617423.4:c.229_236delinsGGGA	ENSP00000478688.1:p.Asn77GlyfsTer?
NM_000488.3:c.229_236delinsGGGA , LRG_577t1:c.229_236delinsGGGA	NP_000479.1:p.Asn77GlyfsTer?
XM_005245198.2:c.85_92delinsGGGA	XP_005245255.1:p.Asn29GlyfsTer?
NM_001365052.1:c.85_92delinsGGGA	NP_001351981.1:p.Asn29GlyfsTer?
NM_000488.4:c.229_236delinsGGGA MANE Select	NP_000479.1:p.Asn77GlyfsTer?
NM_001365052.2:c.85_92delinsGGGA	NP_001351981.1:p.Asn29GlyfsTer?
NM_001386302.1:c.229_236delinsGGGA	NP_001373231.1:p.Asn77GlyfsTer?
NM_001386303.1:c.310_317delinsGGGA	NP_001373232.1:p.Asn104GlyfsTer?
NM_001386304.1:c.229_236delinsGGGA	NP_001373233.1:p.Asn77GlyfsTer?
NM_001386305.1:c.229_236delinsGGGA	NP_001373234.1:p.Asn77GlyfsTer?
NM_001386306.1:c.229_236delinsGGGA	NP_001373235.1:p.Asn77GlyfsTer?