Canonical Allele Identifier: CA2610952524
Gene: HABP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588470_113588471insTGGG , CM000672.2:g.113588470_113588471insTGGG GRCh38
NC_000010.10:g.115348229_115348230insTGGG , CM000672.1:g.115348229_115348230insTGGG GRCh37
NC_000010.9:g.115338219_115338220insTGGG NCBI36
NG_008956.1:g.40452_40453insTGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.*101_*102insTGGG MANE Select ENSP00000277903.4:n.*101_*102insTGGG
ENST00000351270.3:c.*101_*102insTGGG ENSP00000277903.4:n.*101_*102insTGGG
ENST00000542051.5:c.*101_*102insTGGG ENSP00000443283.1:n.*101_*102insTGGG
NM_001177660.1:c.*101_*102insTGGG NP_001171131.1:n.*101_*102insTGGG
NM_004132.3:c.*101_*102insTGGG NP_004123.1:n.*101_*102insTGGG
NM_001177660.2:c.*101_*102insTGGG NP_001171131.1:n.*101_*102insTGGG
NM_004132.4:c.*101_*102insTGGG NP_004123.1:n.*101_*102insTGGG
NM_004132.5:c.*101_*102insTGGG MANE Select NP_004123.1:n.*101_*102insTGGG
NM_001177660.3:c.*101_*102insTGGG NP_001171131.1:n.*101_*102insTGGG