Canonical Allele Identifier: CA1140161197

Gene: INAVA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200908434C= , CM000663.2:g.200908434C=	GRCh38
NC_000001.10:g.200877562C= , CM000663.1:g.200877562C=	GRCh37
NC_000001.9:g.199144185C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413687.3:c.575-296C= MANE Select	ENSP00000392105.2:n.575-296C=
ENST00000367342.8:c.830-296C=	ENSP00000356311.4:n.830-296C=
ENST00000413687.2:c.575-296C=	ENSP00000392105.2:n.575-296C=
NM_001142569.2:c.575-296C=	NP_001136041.1:n.575-296C=
NM_018265.3:c.872-296C=	NP_060735.3:n.872-296C=
XM_011509754.1:c.575-296C=	XP_011508056.1:n.575-296C=
XM_011509755.1:c.575-296C=	XP_011508057.1:n.575-296C=
XM_011509756.1:c.649-296C=	XP_011508058.1:n.649-296C=
XM_011509754.2:c.575-296C=	XP_011508056.1:n.575-296C=
XM_011509756.2:c.649-296C=	XP_011508058.1:n.649-296C=
NM_001142569.3:c.575-296C= MANE Select	NP_001136041.1:n.575-296C=
NM_001367289.1:c.575-296C=	NP_001354218.1:n.575-296C=
NM_001367290.1:c.40-298C=	NP_001354219.1:n.40-298C=
NM_018265.4:c.830-296C=	NP_060735.4:n.830-296C=