Canonical Allele Identifier: CA367069443
Gene: HOXA1 HGNC NCBI

Linked Data

dbSNP Id: rs1167940042
gnomAD v2: 7-27135383-T-C
gnomAD v4: 7-27095764-T-C
MyVariant Identifiers: chr7:g.27135383T>C (hg19) chr7:g.27095764T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095764T>C , CM000669.2:g.27095764T>C GRCh38
NC_000007.13:g.27135383T>C , CM000669.1:g.27135383T>C GRCh37
NC_000007.12:g.27101908T>C NCBI36
NG_011813.1:g.5243A>G
NG_033087.1:g.4671T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.149A>G MANE Select ENSP00000494260.2:p.Asp50Gly
ENST00000343060.4:c.149A>G ENSP00000343246.4:p.Asp50Gly
ENST00000355633.5:c.149A>G ENSP00000347851.5:p.Asp50Gly
NM_005522.4:c.149A>G NP_005513.1:p.Asp50Gly
NM_153620.2:c.149A>G NP_705873.2:p.Asp50Gly
NM_005522.5:c.149A>G MANE Select NP_005513.2:p.Asp50Gly
NM_153620.3:c.149A>G NP_705873.3:p.Asp50Gly
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