Canonical Allele Identifier: CA837187616
Gene: HOXA1 HGNC NCBI

Linked Data

dbSNP Id: rs1312916497
MyVariant Identifiers: chr7:g.27135368del (hg19) chr7:g.27095749del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095749del , CM000669.2:g.27095749del GRCh38
NC_000007.13:g.27135368del , CM000669.1:g.27135368del GRCh37
NC_000007.12:g.27101893del NCBI36
NG_011813.1:g.5258del
NG_033087.1:g.4656del

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.164del MANE Select ENSP00000494260.2:p.Val55GlyfsTer?
ENST00000343060.4:c.164del ENSP00000343246.4:p.Val55GlyfsTer?
ENST00000355633.5:c.164del ENSP00000347851.5:p.Val55GlyfsTer?
NM_005522.4:c.164del NP_005513.1:p.Val55GlyfsTer?
NM_153620.2:c.164del NP_705873.2:p.Val55GlyfsTer?
NM_005522.5:c.164del MANE Select NP_005513.2:p.Val55GlyfsTer?
NM_153620.3:c.164del NP_705873.3:p.Val55GlyfsTer?
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