Canonical Allele Identifier: CA1696187519
Gene: HOXA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095772G= , CM000669.2:g.27095772G= GRCh38
NC_000007.13:g.27135391G= , CM000669.1:g.27135391G= GRCh37
NC_000007.12:g.27101916G= NCBI36
NG_011813.1:g.5235C=
NG_033087.1:g.4679G=

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.141C= MANE Select ENSP00000494260.2:p.Cys47=
ENST00000343060.4:c.141C= ENSP00000343246.4:p.Cys47=
ENST00000355633.5:c.141C= ENSP00000347851.5:p.Cys47=
NM_005522.4:c.141C= NP_005513.1:p.Cys47=
NM_153620.2:c.141C= NP_705873.2:p.Cys47=
NM_005522.5:c.141C= MANE Select NP_005513.2:p.Cys47=
NM_153620.3:c.141C= NP_705873.3:p.Cys47=