Canonical Allele Identifier: CA1207934333

Gene: SERPINC1

Linked Data

• dbSNP Id: rs1657361712

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903824_173903831del , CM000663.2:g.173903824_173903831del	GRCh38
NC_000001.10:g.173872962_173872969del , CM000663.1:g.173872962_173872969del	GRCh37
NC_000001.9:g.172139585_172139592del	NCBI36
NG_012462.1:g.18549_18556del , LRG_577:g.18549_18556del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.*59_*66del MANE Select	ENSP00000356671.3:n.*59_*66del
ENST00000367698.3:c.*59_*66del	ENSP00000356671.3:n.*59_*66del
ENST00000617423.4:c.*59_*66del	ENSP00000478688.1:n.*59_*66del
NM_000488.3:c.*59_*66del , LRG_577t1:c.*59_*66del	NP_000479.1:n.*59_*66del
XM_005245198.2:c.*59_*66del	XP_005245255.1:n.*59_*66del
NM_001365052.1:c.*59_*66del	NP_001351981.1:n.*59_*66del
NM_000488.4:c.*59_*66del MANE Select	NP_000479.1:n.*59_*66del
NM_001365052.2:c.*59_*66del	NP_001351981.1:n.*59_*66del
NM_001386302.1:c.*59_*66del	NP_001373231.1:n.*59_*66del
NM_001386303.1:c.*59_*66del	NP_001373232.1:n.*59_*66del
NM_001386304.1:c.*59_*66del	NP_001373233.1:n.*59_*66del
NM_001386305.1:c.*59_*66del	NP_001373234.1:n.*59_*66del
NM_001386306.1:c.*59_*66del	NP_001373235.1:n.*59_*66del