Canonical Allele Identifier: CA367069458

Gene: HOXA1

Linked Data

• MyVariant Identifiers: chr7:g.27135387C>T (hg19) ; chr7:g.27095768C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.27095768C>T , CM000669.2:g.27095768C>T	GRCh38
NC_000007.13:g.27135387C>T , CM000669.1:g.27135387C>T	GRCh37
NC_000007.12:g.27101912C>T	NCBI36
NG_011813.1:g.5239G>A
NG_033087.1:g.4675C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643460.2:c.145G>A MANE Select	ENSP00000494260.2:p.Gly49Ser
ENST00000343060.4:c.145G>A	ENSP00000343246.4:p.Gly49Ser
ENST00000355633.5:c.145G>A	ENSP00000347851.5:p.Gly49Ser
NM_005522.4:c.145G>A	NP_005513.1:p.Gly49Ser
NM_153620.2:c.145G>A	NP_705873.2:p.Gly49Ser
NM_005522.5:c.145G>A MANE Select	NP_005513.2:p.Gly49Ser
NM_153620.3:c.145G>A	NP_705873.3:p.Gly49Ser