Canonical Allele Identifier: CA1696187083
Gene: HOXA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095623G= , CM000669.2:g.27095623G= GRCh38
NC_000007.13:g.27135242G= , CM000669.1:g.27135242G= GRCh37
NC_000007.12:g.27101767G= NCBI36
NG_011813.1:g.5384C=
NG_033087.1:g.4530G=

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.290C= MANE Select ENSP00000494260.2:p.Pro97=
ENST00000343060.4:c.290C= ENSP00000343246.4:p.Pro97=
ENST00000355633.5:c.290C= ENSP00000347851.5:p.Pro97=
NM_005522.4:c.290C= NP_005513.1:p.Pro97=
NM_153620.2:c.290C= NP_705873.2:p.Pro97=
NM_005522.5:c.290C= MANE Select NP_005513.2:p.Pro97=
NM_153620.3:c.290C= NP_705873.3:p.Pro97=