Canonical Allele Identifier: CA454507665
Gene: HOXA1 HGNC NCBI

Linked Data

dbSNP Id: rs1220099285
gnomAD v2: 7-27135055-G-A
gnomAD v4: 7-27095436-G-A
MyVariant Identifiers: chr7:g.27135055G>A (hg19) chr7:g.27095436G>A (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000643460.2:c.477C>T MANE Select ENSP00000494260.2:p.Tyr159=
ENST00000343060.4:c.477C>T ENSP00000343246.4:p.Tyr159=
ENST00000355633.5:c.355-81C>T ENSP00000347851.5:n.355-81C>T
NM_005522.4:c.477C>T NP_005513.1:p.Tyr159=
NM_153620.2:c.355-81C>T NP_705873.2:n.355-81C>T
NM_005522.5:c.477C>T MANE Select NP_005513.2:p.Tyr159=
NM_153620.3:c.355-81C>T NP_705873.3:n.355-81C>T
Search 100 bp 5'
Search 100 bp 3'