Canonical Allele Identifier: CA367069349
Gene: HOXA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.27135354G>T (hg19) chr7:g.27095735G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095735G>T , CM000669.2:g.27095735G>T GRCh38
NC_000007.13:g.27135354G>T , CM000669.1:g.27135354G>T GRCh37
NC_000007.12:g.27101879G>T NCBI36
NG_011813.1:g.5272C>A
NG_033087.1:g.4642G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.178C>A MANE Select ENSP00000494260.2:p.Gln60Lys
ENST00000343060.4:c.178C>A ENSP00000343246.4:p.Gln60Lys
ENST00000355633.5:c.178C>A ENSP00000347851.5:p.Gln60Lys
NM_005522.4:c.178C>A NP_005513.1:p.Gln60Lys
NM_153620.2:c.178C>A NP_705873.2:p.Gln60Lys
NM_005522.5:c.178C>A MANE Select NP_005513.2:p.Gln60Lys
NM_153620.3:c.178C>A NP_705873.3:p.Gln60Lys
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