Canonical Allele Identifier: CA1009277621

Gene: SERPINC1

Linked Data

• dbSNP Id: rs1657705339
• gnomAD v3: 1-173910108-T-TC
• gnomAD v4: 1-173910108-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173910108_173910109insC , CM000663.2:g.173910108_173910109insC	GRCh38
NC_000001.10:g.173879246_173879247insC , CM000663.1:g.173879246_173879247insC	GRCh37
NC_000001.9:g.172145869_172145870insC	NCBI36
NG_012462.1:g.12270_12271insG , LRG_577:g.12270_12271insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.763-167_763-166insG MANE Select	ENSP00000356671.3:n.763-167_763-166insG
ENST00000367698.3:c.763-167_763-166insG	ENSP00000356671.3:n.763-167_763-166insG
ENST00000487183.1:n.414-167_414-166insG
ENST00000617423.4:c.559+1755_559+1756insG	ENSP00000478688.1:n.559+1755_559+1756insG
NM_000488.3:c.763-167_763-166insG , LRG_577t1:c.763-167_763-166insG	NP_000479.1:n.763-167_763-166insG
XM_005245198.2:c.619-167_619-166insG	XP_005245255.1:n.619-167_619-166insG
NM_001365052.1:c.619-167_619-166insG	NP_001351981.1:n.619-167_619-166insG
NM_000488.4:c.763-167_763-166insG MANE Select	NP_000479.1:n.763-167_763-166insG
NM_001365052.2:c.619-167_619-166insG	NP_001351981.1:n.619-167_619-166insG
NM_001386302.1:c.886-167_886-166insG	NP_001373231.1:n.886-167_886-166insG
NM_001386303.1:c.844-167_844-166insG	NP_001373232.1:n.844-167_844-166insG
NM_001386304.1:c.742-167_742-166insG	NP_001373233.1:n.742-167_742-166insG
NM_001386305.1:c.763-224_763-223insG	NP_001373234.1:n.763-224_763-223insG
NM_001386306.1:c.547-167_547-166insG	NP_001373235.1:n.547-167_547-166insG