Canonical Allele Identifier: CA1696186900
Gene: HOXA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095453C= , CM000669.2:g.27095453C= GRCh38
NC_000007.13:g.27135072C= , CM000669.1:g.27135072C= GRCh37
NC_000007.12:g.27101597C= NCBI36
NG_011813.1:g.5554G=
NG_033087.1:g.4360C=

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.460G= MANE Select ENSP00000494260.2:p.Val154=
ENST00000343060.4:c.460G= ENSP00000343246.4:p.Val154=
ENST00000355633.5:c.355-98G= ENSP00000347851.5:n.355-98G=
NM_005522.4:c.460G= NP_005513.1:p.Val154=
NM_153620.2:c.355-98G= NP_705873.2:n.355-98G=
NM_005522.5:c.460G= MANE Select NP_005513.2:p.Val154=
NM_153620.3:c.355-98G= NP_705873.3:n.355-98G=