Canonical Allele Identifier: CA10625947
Gene: HOXA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 359964
ClinVar RCV Id: RCV000264065
dbSNP Id: rs886062259
MyVariant Identifiers: chr7:g.27135277G>C (hg19) chr7:g.27095658G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095658G>C , CM000669.2:g.27095658G>C GRCh38
NC_000007.13:g.27135277G>C , CM000669.1:g.27135277G>C GRCh37
NC_000007.12:g.27101802G>C NCBI36
NG_011813.1:g.5349C>G
NG_033087.1:g.4565G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000643460.2:c.255C>G MANE Select ENSP00000494260.2:p.Asn85Lys
ENST00000343060.4:c.255C>G ENSP00000343246.4:p.Asn85Lys
ENST00000355633.5:c.255C>G ENSP00000347851.5:p.Asn85Lys
NM_005522.4:c.255C>G NP_005513.1:p.Asn85Lys
NM_153620.2:c.255C>G NP_705873.2:p.Asn85Lys
NM_005522.5:c.255C>G MANE Select NP_005513.2:p.Asn85Lys
NM_153620.3:c.255C>G NP_705873.3:p.Asn85Lys
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