Canonical Allele Identifier: CA918764873
Gene: HABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1276883379

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588288dup , CM000672.2:g.113588288dup GRCh38
NC_000010.10:g.115348047dup , CM000672.1:g.115348047dup GRCh37
NC_000010.9:g.115338037dup NCBI36
NG_008956.1:g.40270dup

Transcript Alleles

HGVS Amino-acid change
ENST00000351270.4:c.1602dup MANE Select ENSP00000277903.4:p.Lys535GlufsTer23
ENST00000351270.3:c.1602dup ENSP00000277903.4:p.Lys535GlufsTer23
ENST00000542051.5:c.1524dup ENSP00000443283.1:p.Lys509GlufsTer23
NM_001177660.1:c.1524dup NP_001171131.1:p.Lys509GlufsTer23
NM_004132.3:c.1602dup NP_004123.1:p.Lys535GlufsTer23
NM_001177660.2:c.1524dup NP_001171131.1:p.Lys509GlufsTer23
NM_004132.4:c.1602dup NP_004123.1:p.Lys535GlufsTer23
NM_004132.5:c.1602dup MANE Select NP_004123.1:p.Lys535GlufsTer23
NM_001177660.3:c.1524dup NP_001171131.1:p.Lys509GlufsTer23