Canonical Allele Identifier: CA1703472877

Gene: BLVRA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.43788099_43788100delinsAT , CM000669.2:g.43788099_43788100delinsAT	GRCh38
NC_000007.13:g.43827698_43827699delinsAT , CM000669.1:g.43827698_43827699delinsAT	GRCh37
NC_000007.12:g.43794223_43794224delinsAT	NCBI36
NG_031876.1:g.34427_34428delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265523.9:c.134+74_134+75delinsAT MANE Select	ENSP00000265523.4:n.134+74_134+75delinsAT
ENST00000265523.8:c.134+74_134+75delinsAT	ENSP00000265523.4:n.134+74_134+75delinsAT
ENST00000402924.5:c.134+74_134+75delinsAT	ENSP00000385757.1:n.134+74_134+75delinsAT
ENST00000424330.1:c.134+74_134+75delinsAT	ENSP00000412005.1:n.134+74_134+75delinsAT
ENST00000453612.1:n.158+74_158+75delinsAT
NM_000712.3:c.134+74_134+75delinsAT	NP_000703.2:n.134+74_134+75delinsAT
NM_001253823.1:c.134+74_134+75delinsAT	NP_001240752.1:n.134+74_134+75delinsAT
XM_011515474.1:c.134+74_134+75delinsAT	XP_011513776.1:n.134+74_134+75delinsAT
XR_428136.2:n.265-2342_265-2341delinsAT
XR_927212.1:n.265-2342_265-2341delinsAT
XR_927213.1:n.265-2342_265-2341delinsAT
XM_011515474.3:c.134+74_134+75delinsAT	XP_011513776.1:n.134+74_134+75delinsAT
XM_017012520.2:c.134+74_134+75delinsAT	XP_016868009.1:n.134+74_134+75delinsAT
XM_024446867.1:c.134+74_134+75delinsAT	XP_024302635.1:n.134+74_134+75delinsAT
XR_001745190.1:n.266-2342_266-2341delinsAT
NM_000712.4:c.134+74_134+75delinsAT MANE Select	NP_000703.2:n.134+74_134+75delinsAT
NM_001253823.2:c.134+74_134+75delinsAT	NP_001240752.1:n.134+74_134+75delinsAT