Canonical Allele Identifier: CA1703472852

Gene: BLVRA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.43788043T= , CM000669.2:g.43788043T=	GRCh38
NC_000007.13:g.43827642T= , CM000669.1:g.43827642T=	GRCh37
NC_000007.12:g.43794167T=	NCBI36
NG_031876.1:g.34371T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265523.9:c.134+18T= MANE Select	ENSP00000265523.4:n.134+18T=
ENST00000265523.8:c.134+18T=	ENSP00000265523.4:n.134+18T=
ENST00000402924.5:c.134+18T=	ENSP00000385757.1:n.134+18T=
ENST00000424330.1:c.134+18T=	ENSP00000412005.1:n.134+18T=
ENST00000453612.1:n.158+18T=
NM_000712.3:c.134+18T=	NP_000703.2:n.134+18T=
NM_001253823.1:c.134+18T=	NP_001240752.1:n.134+18T=
XM_011515474.1:c.134+18T=	XP_011513776.1:n.134+18T=
XR_428136.2:n.265-2285A=
XR_927212.1:n.265-2285A=
XR_927213.1:n.265-2285A=
XM_011515474.3:c.134+18T=	XP_011513776.1:n.134+18T=
XM_017012520.2:c.134+18T=	XP_016868009.1:n.134+18T=
XM_024446867.1:c.134+18T=	XP_024302635.1:n.134+18T=
XR_001745190.1:n.266-2285A=
NM_000712.4:c.134+18T= MANE Select	NP_000703.2:n.134+18T=
NM_001253823.2:c.134+18T=	NP_001240752.1:n.134+18T=