Canonical Allele Identifier: CA1696186888
Gene: HOXA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095436G= , CM000669.2:g.27095436G= GRCh38
NC_000007.13:g.27135055G= , CM000669.1:g.27135055G= GRCh37
NC_000007.12:g.27101580G= NCBI36
NG_011813.1:g.5571C=
NG_033087.1:g.4343G=

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.477C= MANE Select ENSP00000494260.2:p.Tyr159=
ENST00000343060.4:c.477C= ENSP00000343246.4:p.Tyr159=
ENST00000355633.5:c.355-81C= ENSP00000347851.5:n.355-81C=
NM_005522.4:c.477C= NP_005513.1:p.Tyr159=
NM_153620.2:c.355-81C= NP_705873.2:n.355-81C=
NM_005522.5:c.477C= MANE Select NP_005513.2:p.Tyr159=
NM_153620.3:c.355-81C= NP_705873.3:n.355-81C=