Canonical Allele Identifier: CA1937420565
Gene: HABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1845302337

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113571203del , CM000672.2:g.113571203del GRCh38
NC_000010.10:g.115330962del , CM000672.1:g.115330962del GRCh37
NC_000010.9:g.115320952del NCBI36
NG_008956.1:g.23185del

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.107-3086del MANE Select ENSP00000277903.4:n.107-3086del
ENST00000351270.3:c.107-3086del ENSP00000277903.4:n.107-3086del
ENST00000542051.5:c.29-3086del ENSP00000443283.1:n.29-3086del
NM_001177660.1:c.29-3086del NP_001171131.1:n.29-3086del
NM_004132.3:c.107-3086del NP_004123.1:n.107-3086del
NM_001177660.2:c.29-3086del NP_001171131.1:n.29-3086del
NM_004132.4:c.107-3086del NP_004123.1:n.107-3086del
NM_004132.5:c.107-3086del MANE Select NP_004123.1:n.107-3086del
NM_001177660.3:c.29-3086del NP_001171131.1:n.29-3086del