Canonical Allele Identifier: CA1207937650

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173911383_173911385delinsCAG , CM000663.2:g.173911383_173911385delinsCAG	GRCh38
NC_000001.10:g.173880521_173880523delinsCAG , CM000663.1:g.173880521_173880523delinsCAG	GRCh37
NC_000001.9:g.172147144_172147146delinsCAG	NCBI36
NG_012462.1:g.10994_10996delinsCTG , LRG_577:g.10994_10996delinsCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.624+414_624+416delinsCTG MANE Select	ENSP00000356671.3:n.624+414_624+416delinsCTG
ENST00000367698.3:c.624+414_624+416delinsCTG	ENSP00000356671.3:n.624+414_624+416delinsCTG
ENST00000487183.1:n.329+414_329+416delinsCTG
ENST00000617423.4:c.559+479_559+481delinsCTG	ENSP00000478688.1:n.559+479_559+481delinsCTG
NM_000488.3:c.624+414_624+416delinsCTG , LRG_577t1:c.624+414_624+416delinsCTG	NP_000479.1:n.624+414_624+416delinsCTG
XM_005245198.2:c.480+414_480+416delinsCTG	XP_005245255.1:n.480+414_480+416delinsCTG
NM_001365052.1:c.480+414_480+416delinsCTG	NP_001351981.1:n.480+414_480+416delinsCTG
NM_000488.4:c.624+414_624+416delinsCTG MANE Select	NP_000479.1:n.624+414_624+416delinsCTG
NM_001365052.2:c.480+414_480+416delinsCTG	NP_001351981.1:n.480+414_480+416delinsCTG
NM_001386302.1:c.624+414_624+416delinsCTG	NP_001373231.1:n.624+414_624+416delinsCTG
NM_001386303.1:c.705+414_705+416delinsCTG	NP_001373232.1:n.705+414_705+416delinsCTG
NM_001386304.1:c.624+414_624+416delinsCTG	NP_001373233.1:n.624+414_624+416delinsCTG
NM_001386305.1:c.624+414_624+416delinsCTG	NP_001373234.1:n.624+414_624+416delinsCTG
NM_001386306.1:c.409-494_409-492delinsCTG	NP_001373235.1:n.409-494_409-492delinsCTG