Canonical Allele Identifier: CA214431721

Gene: HABP2

Linked Data

• dbSNP Id: rs370471925

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113571078_113571080del , CM000672.2:g.113571078_113571080del	GRCh38
NC_000010.10:g.115330837_115330839del , CM000672.1:g.115330837_115330839del	GRCh37
NC_000010.9:g.115320827_115320829del	NCBI36
NG_008956.1:g.23060_23062del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.107-3211_107-3209del MANE Select	ENSP00000277903.4:n.107-3211_107-3209del
ENST00000351270.3:c.107-3211_107-3209del	ENSP00000277903.4:n.107-3211_107-3209del
ENST00000542051.5:c.29-3211_29-3209del	ENSP00000443283.1:n.29-3211_29-3209del
NM_001177660.1:c.29-3211_29-3209del	NP_001171131.1:n.29-3211_29-3209del
NM_004132.3:c.107-3211_107-3209del	NP_004123.1:n.107-3211_107-3209del
NM_001177660.2:c.29-3211_29-3209del	NP_001171131.1:n.29-3211_29-3209del
NM_004132.4:c.107-3211_107-3209del	NP_004123.1:n.107-3211_107-3209del
NM_004132.5:c.107-3211_107-3209del MANE Select	NP_004123.1:n.107-3211_107-3209del
NM_001177660.3:c.29-3211_29-3209del	NP_001171131.1:n.29-3211_29-3209del