Canonical Allele Identifier: CA1937429181
Gene: HABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588296C= , CM000672.2:g.113588296C= GRCh38
NC_000010.10:g.115348055C= , CM000672.1:g.115348055C= GRCh37
NC_000010.9:g.115338045C= NCBI36
NG_008956.1:g.40278C=

Transcript Alleles

HGVS Amino-acid change
ENST00000351270.4:c.1610C= MANE Select ENSP00000277903.4:p.Pro537=
ENST00000351270.3:c.1610C= ENSP00000277903.4:p.Pro537=
ENST00000542051.5:c.1532C= ENSP00000443283.1:p.Pro511=
NM_001177660.1:c.1532C= NP_001171131.1:p.Pro511=
NM_004132.3:c.1610C= NP_004123.1:p.Pro537=
NM_001177660.2:c.1532C= NP_001171131.1:p.Pro511=
NM_004132.4:c.1610C= NP_004123.1:p.Pro537=
NM_004132.5:c.1610C= MANE Select NP_004123.1:p.Pro537=
NM_001177660.3:c.1532C= NP_001171131.1:p.Pro511=