Canonical Allele Identifier: CA454507859
Gene: HOXA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.27135370T>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095751T>G , CM000669.2:g.27095751T>G GRCh38
NC_000007.13:g.27135370T>G , CM000669.1:g.27135370T>G GRCh37
NC_000007.12:g.27101895T>G NCBI36
NG_011813.1:g.5256A>C
NG_033087.1:g.4658T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.162A>C MANE Select ENSP00000494260.2:p.Leu54=
ENST00000343060.4:c.162A>C ENSP00000343246.4:p.Leu54=
ENST00000355633.5:c.162A>C ENSP00000347851.5:p.Leu54=
NM_005522.4:c.162A>C NP_005513.1:p.Leu54=
NM_153620.2:c.162A>C NP_705873.2:p.Leu54=
NM_005522.5:c.162A>C MANE Select NP_005513.2:p.Leu54=
NM_153620.3:c.162A>C NP_705873.3:p.Leu54=
Search 100 bp 5'
Search 100 bp 3'