Canonical Allele Identifier: CA1703472844
Gene: BLVRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.43788025_43788027delinsGGT , CM000669.2:g.43788025_43788027delinsGGT GRCh38
NC_000007.13:g.43827624_43827626delinsGGT , CM000669.1:g.43827624_43827626delinsGGT GRCh37
NC_000007.12:g.43794149_43794151delinsGGT NCBI36
NG_031876.1:g.34353_34355delinsGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265523.9:c.134_134+2delinsGGT
ENST00000265523.8:c.134_134+2delinsGGT
ENST00000402924.5:c.134_134+2delinsGGT
ENST00000424330.1:c.134_134+2delinsGGT
ENST00000453612.1:n.158_158+2delinsGGT
NM_000712.3:c.134_134+2delinsGGT
NM_001253823.1:c.134_134+2delinsGGT
XM_011515474.1:c.134_134+2delinsGGT
XR_428136.2:n.265-2269_265-2267delinsACC
XR_927212.1:n.265-2269_265-2267delinsACC
XR_927213.1:n.265-2269_265-2267delinsACC
XM_011515474.3:c.134_134+2delinsGGT
XM_017012520.2:c.134_134+2delinsGGT
XM_024446867.1:c.134_134+2delinsGGT
XR_001745190.1:n.266-2269_266-2267delinsACC
NM_000712.4:c.134_134+2delinsGGT
NM_001253823.2:c.134_134+2delinsGGT