Canonical Allele Identifier: CA1207936950

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909680_173909684delinsTCATC , CM000663.2:g.173909680_173909684delinsTCATC	GRCh38
NC_000001.10:g.173878818_173878822delinsTCATC , CM000663.1:g.173878818_173878822delinsTCATC	GRCh37
NC_000001.9:g.172145441_172145445delinsTCATC	NCBI36
NG_012462.1:g.12695_12699delinsGATGA , LRG_577:g.12695_12699delinsGATGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1021_1025delinsGATGA MANE Select	ENSP00000356671.3:p.Asp341=
ENST00000367698.3:c.1021_1025delinsGATGA	ENSP00000356671.3:p.Asp341=
ENST00000617423.4:c.559+2180_559+2184delinsGATGA	ENSP00000478688.1:n.559+2180_559+2184delinsGATGA
NM_000488.3:c.1021_1025delinsGATGA , LRG_577t1:c.1021_1025delinsGATGA	NP_000479.1:p.Asp341=
XM_005245198.2:c.877_881delinsGATGA	XP_005245255.1:p.Asp293=
NM_001365052.1:c.877_881delinsGATGA	NP_001351981.1:p.Asp293=
NM_000488.4:c.1021_1025delinsGATGA MANE Select	NP_000479.1:p.Asp341=
NM_001365052.2:c.877_881delinsGATGA	NP_001351981.1:p.Asp293=
NM_001386302.1:c.1144_1148delinsGATGA	NP_001373231.1:p.Asp382=
NM_001386303.1:c.1102_1106delinsGATGA	NP_001373232.1:p.Asp368=
NM_001386304.1:c.1000_1004delinsGATGA	NP_001373233.1:p.Asp334=
NM_001386305.1:c.964_968delinsGATGA	NP_001373234.1:p.Asp322=
NM_001386306.1:c.805_809delinsGATGA	NP_001373235.1:p.Asp269=