Canonical Allele Identifier: CA367069373

Gene: HOXA1

Linked Data

• MyVariant Identifiers: chr7:g.27135362C>G (hg19) ; chr7:g.27095743C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.27095743C>G , CM000669.2:g.27095743C>G	GRCh38
NC_000007.13:g.27135362C>G , CM000669.1:g.27135362C>G	GRCh37
NC_000007.12:g.27101887C>G	NCBI36
NG_011813.1:g.5264G>C
NG_033087.1:g.4650C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643460.2:c.170G>C MANE Select	ENSP00000494260.2:p.Arg57Thr
ENST00000343060.4:c.170G>C	ENSP00000343246.4:p.Arg57Thr
ENST00000355633.5:c.170G>C	ENSP00000347851.5:p.Arg57Thr
NM_005522.4:c.170G>C	NP_005513.1:p.Arg57Thr
NM_153620.2:c.170G>C	NP_705873.2:p.Arg57Thr
NM_005522.5:c.170G>C MANE Select	NP_005513.2:p.Arg57Thr
NM_153620.3:c.170G>C	NP_705873.3:p.Arg57Thr