Canonical Allele Identifier: CA378422293

Gene: HABP2

Linked Data

• MyVariant Identifiers: chr10:g.115348065C>A (hg19) ; chr10:g.113588306C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588306C>A , CM000672.2:g.113588306C>A	GRCh38
NC_000010.10:g.115348065C>A , CM000672.1:g.115348065C>A	GRCh37
NC_000010.9:g.115338055C>A	NCBI36
NG_008956.1:g.40288C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.1620C>A MANE Select	ENSP00000277903.4:p.Tyr540Ter
ENST00000351270.3:c.1620C>A	ENSP00000277903.4:p.Tyr540Ter
ENST00000542051.5:c.1542C>A	ENSP00000443283.1:p.Tyr514Ter
NM_001177660.1:c.1542C>A	NP_001171131.1:p.Tyr514Ter
NM_004132.3:c.1620C>A	NP_004123.1:p.Tyr540Ter
NM_001177660.2:c.1542C>A	NP_001171131.1:p.Tyr514Ter
NM_004132.4:c.1620C>A	NP_004123.1:p.Tyr540Ter
NM_004132.5:c.1620C>A MANE Select	NP_004123.1:p.Tyr540Ter
NM_001177660.3:c.1542C>A	NP_001171131.1:p.Tyr514Ter