Canonical Allele Identifier: CA1143355585
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173914725_173914732delinsCGCCGGTT , CM000663.2:g.173914725_173914732delinsCGCCGGTT GRCh38
NC_000001.10:g.173883863_173883870delinsCGCCGGTT , CM000663.1:g.173883863_173883870delinsCGCCGGTT GRCh37
NC_000001.9:g.172150486_172150493delinsCGCCGGTT NCBI36
NG_012462.1:g.7647_7654delinsAACCGGCG , LRG_577:g.7647_7654delinsAACCGGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.229_236delinsAACCGGCG MANE Select ENSP00000356671.3:p.Asn77=
ENST00000367698.3:c.229_236delinsAACCGGCG ENSP00000356671.3:p.Asn77=
ENST00000494024.1:n.455_462delinsAACCGGCG
ENST00000617423.4:c.229_236delinsAACCGGCG ENSP00000478688.1:p.Asn77=
NM_000488.3:c.229_236delinsAACCGGCG , LRG_577t1:c.229_236delinsAACCGGCG NP_000479.1:p.Asn77=
XM_005245198.2:c.85_92delinsAACCGGCG XP_005245255.1:p.Asn29=
NM_001365052.1:c.85_92delinsAACCGGCG NP_001351981.1:p.Asn29=
NM_000488.4:c.229_236delinsAACCGGCG MANE Select NP_000479.1:p.Asn77=
NM_001365052.2:c.85_92delinsAACCGGCG NP_001351981.1:p.Asn29=
NM_001386302.1:c.229_236delinsAACCGGCG NP_001373231.1:p.Asn77=
NM_001386303.1:c.310_317delinsAACCGGCG NP_001373232.1:p.Asn104=
NM_001386304.1:c.229_236delinsAACCGGCG NP_001373233.1:p.Asn77=
NM_001386305.1:c.229_236delinsAACCGGCG NP_001373234.1:p.Asn77=
NM_001386306.1:c.229_236delinsAACCGGCG NP_001373235.1:p.Asn77=