Canonical Allele Identifier: CA1937429274
Gene: HABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588446_113588455delinsACCTCCAGAG , CM000672.2:g.113588446_113588455delinsACCTCCAGAG GRCh38
NC_000010.10:g.115348205_115348214delinsACCTCCAGAG , CM000672.1:g.115348205_115348214delinsACCTCCAGAG GRCh37
NC_000010.9:g.115338195_115338204delinsACCTCCAGAG NCBI36
NG_008956.1:g.40428_40437delinsACCTCCAGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.*77_*86delinsACCTCCAGAG MANE Select ENSP00000277903.4:n.*77_*86delinsACCTCCAGAG
ENST00000351270.3:c.*77_*86delinsACCTCCAGAG ENSP00000277903.4:n.*77_*86delinsACCTCCAGAG
ENST00000542051.5:c.*77_*86delinsACCTCCAGAG ENSP00000443283.1:n.*77_*86delinsACCTCCAGAG
NM_001177660.1:c.*77_*86delinsACCTCCAGAG NP_001171131.1:n.*77_*86delinsACCTCCAGAG
NM_004132.3:c.*77_*86delinsACCTCCAGAG NP_004123.1:n.*77_*86delinsACCTCCAGAG
NM_001177660.2:c.*77_*86delinsACCTCCAGAG NP_001171131.1:n.*77_*86delinsACCTCCAGAG
NM_004132.4:c.*77_*86delinsACCTCCAGAG NP_004123.1:n.*77_*86delinsACCTCCAGAG
NM_004132.5:c.*77_*86delinsACCTCCAGAG MANE Select NP_004123.1:n.*77_*86delinsACCTCCAGAG
NM_001177660.3:c.*77_*86delinsACCTCCAGAG NP_001171131.1:n.*77_*86delinsACCTCCAGAG