Canonical Allele Identifier: CA1703479010

Gene: BLVRA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.43803185C= , CM000669.2:g.43803185C=	GRCh38
NC_000007.13:g.43842784C= , CM000669.1:g.43842784C=	GRCh37
NC_000007.12:g.43809309C=	NCBI36
NG_031876.1:g.49513C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000712.4:c.461-491C= MANE Select	NP_000703.2:n.461-491C=
ENST00000265523.9:c.461-491C= MANE Select	ENSP00000265523.4:n.461-491C=
NM_000712.3:c.461-491C=	NP_000703.2:n.461-491C=
NM_001253823.1:c.461-491C=	NP_001240752.1:n.461-491C=
NM_001253823.2:c.461-491C=	NP_001240752.1:n.461-491C=
ENST00000265523.8:c.461-491C=	ENSP00000265523.4:n.461-491C=
ENST00000402924.5:c.461-491C=	ENSP00000385757.1:n.461-491C=
ENST00000486984.1:n.165-491C=
XM_011515474.1:c.461-491C=	XP_011513776.1:n.461-491C=
XM_011515474.3:c.461-491C=	XP_011513776.1:n.461-491C=
XM_017012520.2:c.461-491C=	XP_016868009.1:n.461-491C=
XM_024446867.1:c.461-491C=	XP_024302635.1:n.461-491C=
XR_001745190.1:n.266-17427G=
XR_428136.2:n.265-17427G=
XR_927212.1:n.265-17427G=
XR_927213.1:n.265-17427G=