Canonical Allele Identifier: CA378422122

Gene: HABP2

Linked Data

• MyVariant Identifiers: chr10:g.115348030T>G (hg19) ; chr10:g.113588271T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588271T>G , CM000672.2:g.113588271T>G	GRCh38
NC_000010.10:g.115348030T>G , CM000672.1:g.115348030T>G	GRCh37
NC_000010.9:g.115338020T>G	NCBI36
NG_008956.1:g.40253T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.1585T>G MANE Select	ENSP00000277903.4:p.Trp529Gly
ENST00000351270.3:c.1585T>G	ENSP00000277903.4:p.Trp529Gly
ENST00000542051.5:c.1507T>G	ENSP00000443283.1:p.Trp503Gly
NM_001177660.1:c.1507T>G	NP_001171131.1:p.Trp503Gly
NM_004132.3:c.1585T>G	NP_004123.1:p.Trp529Gly
NM_001177660.2:c.1507T>G	NP_001171131.1:p.Trp503Gly
NM_004132.4:c.1585T>G	NP_004123.1:p.Trp529Gly
NM_004132.5:c.1585T>G MANE Select	NP_004123.1:p.Trp529Gly
NM_001177660.3:c.1507T>G	NP_001171131.1:p.Trp503Gly