Canonical Allele Identifier: CA367069035

Gene: HOXA1

Linked Data

• MyVariant Identifiers: chr7:g.27135273C>A (hg19) ; chr7:g.27095654C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.27095654C>A , CM000669.2:g.27095654C>A	GRCh38
NC_000007.13:g.27135273C>A , CM000669.1:g.27135273C>A	GRCh37
NC_000007.12:g.27101798C>A	NCBI36
NG_011813.1:g.5353G>T
NG_033087.1:g.4561C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643460.2:c.259G>T MANE Select	ENSP00000494260.2:p.Gly87Trp
ENST00000343060.4:c.259G>T	ENSP00000343246.4:p.Gly87Trp
ENST00000355633.5:c.259G>T	ENSP00000347851.5:p.Gly87Trp
NM_005522.4:c.259G>T	NP_005513.1:p.Gly87Trp
NM_153620.2:c.259G>T	NP_705873.2:p.Gly87Trp
NM_005522.5:c.259G>T MANE Select	NP_005513.2:p.Gly87Trp
NM_153620.3:c.259G>T	NP_705873.3:p.Gly87Trp