Canonical Allele Identifier: CA4195996

Gene: HOXA1

Linked Data

• dbSNP Id: rs747464910
• ExAC: 7:27135316 ATGGTGGTGG / A
• gnomAD v2: 7-27135316-ATGGTGGTGG-A
• gnomAD v3: 7-27095697-ATGGTGGTGG-A
• gnomAD v4: 7-27095697-ATGGTGGTGG-A
• COSMIC: COSM4168153
• MyVariant Identifiers: chr7:g.27135317_27135325del (hg19) ; chr7:g.27095698_27095706del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.27095713_27095721del , CM000669.2:g.27095713_27095721del	GRCh38
NC_000007.13:g.27135332_27135340del , CM000669.1:g.27135332_27135340del	GRCh37
NC_000007.12:g.27101857_27101865del	NCBI36
NG_011813.1:g.5301_5309del
NG_033087.1:g.4620_4628del

Transcript Alleles

HGVS	Amino-acid change
ENST00000643460.2:c.207_215del MANE Select	ENSP00000494260.2:p.His70_His72del
ENST00000343060.4:c.207_215del	ENSP00000343246.4:p.His70_His72del
ENST00000355633.5:c.207_215del	ENSP00000347851.5:p.His70_His72del
NM_005522.4:c.207_215del	NP_005513.1:p.His70_His72del
NM_153620.2:c.207_215del	NP_705873.2:p.His70_His72del
NM_005522.5:c.207_215del MANE Select	NP_005513.2:p.His70_His72del
NM_153620.3:c.207_215del	NP_705873.3:p.His70_His72del