Canonical Allele Identifier: CA2994137142

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903974_173903976del , CM000663.2:g.173903974_173903976del	GRCh38
NC_000001.10:g.173873112_173873114del , CM000663.1:g.173873112_173873114del	GRCh37
NC_000001.9:g.172139735_172139737del	NCBI36
NG_012462.1:g.18405_18407del , LRG_577:g.18405_18407del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1310_1312del MANE Select	ENSP00000356671.3:p.Asn437del
ENST00000367698.3:c.1310_1312del	ENSP00000356671.3:p.Asn437del
ENST00000617423.4:c.695_697del	ENSP00000478688.1:p.Asn232del
NM_000488.3:c.1310_1312del , LRG_577t1:c.1310_1312del	NP_000479.1:p.Asn437del
XM_005245198.2:c.1166_1168del	XP_005245255.1:p.Asn389del
NM_001365052.1:c.1166_1168del	NP_001351981.1:p.Asn389del
NM_000488.4:c.1310_1312del MANE Select	NP_000479.1:p.Asn437del
NM_001365052.2:c.1166_1168del	NP_001351981.1:p.Asn389del
NM_001386302.1:c.1433_1435del	NP_001373231.1:p.Asn478del
NM_001386303.1:c.1391_1393del	NP_001373232.1:p.Asn464del
NM_001386304.1:c.1289_1291del	NP_001373233.1:p.Asn430del
NM_001386305.1:c.1253_1255del	NP_001373234.1:p.Asn418del
NM_001386306.1:c.1094_1096del	NP_001373235.1:p.Asn365del