Canonical Allele Identifier: CA4195934
Gene: HOXA1 HGNC NCBI

Linked Data

dbSNP Id: rs371627984
ExAC: 7:27135073 C / T
gnomAD v2: 7-27135073-C-T
gnomAD v4: 7-27095454-C-T
MyVariant Identifiers: chr7:g.27135073C>T (hg19) chr7:g.27095454C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095454C>T , CM000669.2:g.27095454C>T GRCh38
NC_000007.13:g.27135073C>T , CM000669.1:g.27135073C>T GRCh37
NC_000007.12:g.27101598C>T NCBI36
NG_011813.1:g.5553G>A
NG_033087.1:g.4361C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000643460.2:c.459G>A MANE Select ENSP00000494260.2:p.Ala153=
ENST00000343060.4:c.459G>A ENSP00000343246.4:p.Ala153=
ENST00000355633.5:c.355-99G>A ENSP00000347851.5:n.355-99G>A
NM_005522.4:c.459G>A NP_005513.1:p.Ala153=
NM_153620.2:c.355-99G>A NP_705873.2:n.355-99G>A
NM_005522.5:c.459G>A MANE Select NP_005513.2:p.Ala153=
NM_153620.3:c.355-99G>A NP_705873.3:n.355-99G>A
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