Canonical Allele Identifier: CA367068416

Gene: HOXA1

Linked Data

• MyVariant Identifiers: chr7:g.27135025C>A (hg19) ; chr7:g.27095406C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.27095406C>A , CM000669.2:g.27095406C>A	GRCh38
NC_000007.13:g.27135025C>A , CM000669.1:g.27135025C>A	GRCh37
NC_000007.12:g.27101550C>A	NCBI36
NG_011813.1:g.5601G>T
NG_033087.1:g.4313C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643460.2:c.507G>T MANE Select	ENSP00000494260.2:p.Gln169His
ENST00000343060.4:c.507G>T	ENSP00000343246.4:p.Gln169His
ENST00000355633.5:c.355-51G>T	ENSP00000347851.5:n.355-51G>T
NM_005522.4:c.507G>T	NP_005513.1:p.Gln169His
NM_153620.2:c.355-51G>T	NP_705873.2:n.355-51G>T
NM_005522.5:c.507G>T MANE Select	NP_005513.2:p.Gln169His
NM_153620.3:c.355-51G>T	NP_705873.3:n.355-51G>T