Canonical Allele Identifier: CA2649174490

Gene: SERPINC1

Linked Data

• gnomAD v4: 1-173911656-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173911658dup , CM000663.2:g.173911658dup	GRCh38
NC_000001.10:g.173880796dup , CM000663.1:g.173880796dup	GRCh37
NC_000001.9:g.172147419dup	NCBI36
NG_012462.1:g.10722dup , LRG_577:g.10722dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.624+142dup MANE Select	ENSP00000356671.3:n.624+142dup
ENST00000367698.3:c.624+142dup	ENSP00000356671.3:n.624+142dup
ENST00000487183.1:n.329+142dup
ENST00000617423.4:c.559+207dup	ENSP00000478688.1:n.559+207dup
NM_000488.3:c.624+142dup , LRG_577t1:c.624+142dup	NP_000479.1:n.624+142dup
XM_005245198.2:c.480+142dup	XP_005245255.1:n.480+142dup
NM_001365052.1:c.480+142dup	NP_001351981.1:n.480+142dup
NM_000488.4:c.624+142dup MANE Select	NP_000479.1:n.624+142dup
NM_001365052.2:c.480+142dup	NP_001351981.1:n.480+142dup
NM_001386302.1:c.624+142dup	NP_001373231.1:n.624+142dup
NM_001386303.1:c.705+142dup	NP_001373232.1:n.705+142dup
NM_001386304.1:c.624+142dup	NP_001373233.1:n.624+142dup
NM_001386305.1:c.624+142dup	NP_001373234.1:n.624+142dup
NM_001386306.1:c.409-766dup	NP_001373235.1:n.409-766dup