Canonical Allele Identifier: CA378421990

Gene: HABP2

Linked Data

• MyVariant Identifiers: chr10:g.115347985A>T (hg19) ; chr10:g.113588226A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588226A>T , CM000672.2:g.113588226A>T	GRCh38
NC_000010.10:g.115347985A>T , CM000672.1:g.115347985A>T	GRCh37
NC_000010.9:g.115337975A>T	NCBI36
NG_008956.1:g.40208A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.1540A>T MANE Select	ENSP00000277903.4:p.Thr514Ser
ENST00000351270.3:c.1540A>T	ENSP00000277903.4:p.Thr514Ser
ENST00000542051.5:c.1462A>T	ENSP00000443283.1:p.Thr488Ser
NM_001177660.1:c.1462A>T	NP_001171131.1:p.Thr488Ser
NM_004132.3:c.1540A>T	NP_004123.1:p.Thr514Ser
NM_001177660.2:c.1462A>T	NP_001171131.1:p.Thr488Ser
NM_004132.4:c.1540A>T	NP_004123.1:p.Thr514Ser
NM_004132.5:c.1540A>T MANE Select	NP_004123.1:p.Thr514Ser
NM_001177660.3:c.1462A>T	NP_001171131.1:p.Thr488Ser