Canonical Allele Identifier: CA367068719

Gene: HOXA1

Linked Data

• MyVariant Identifiers: chr7:g.27135164T>A (hg19) ; chr7:g.27095545T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.27095545T>A , CM000669.2:g.27095545T>A	GRCh38
NC_000007.13:g.27135164T>A , CM000669.1:g.27135164T>A	GRCh37
NC_000007.12:g.27101689T>A	NCBI36
NG_011813.1:g.5462A>T
NG_033087.1:g.4452T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643460.2:c.368A>T MANE Select	ENSP00000494260.2:p.Tyr123Phe
ENST00000343060.4:c.368A>T	ENSP00000343246.4:p.Tyr123Phe
ENST00000355633.5:c.354+14A>T	ENSP00000347851.5:n.354+14A>T
NM_005522.4:c.368A>T	NP_005513.1:p.Tyr123Phe
NM_153620.2:c.354+14A>T	NP_705873.2:n.354+14A>T
NM_005522.5:c.368A>T MANE Select	NP_005513.2:p.Tyr123Phe
NM_153620.3:c.354+14A>T	NP_705873.3:n.354+14A>T