Canonical Allele Identifier: CA338193101

Gene: H6PD

Linked Data

• MyVariant Identifiers: chr1:g.9324014C>A (hg19) ; chr1:g.9263955C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.9263955C>A , CM000663.2:g.9263955C>A	GRCh38
NC_000001.10:g.9324014C>A , CM000663.1:g.9324014C>A	GRCh37
NC_000001.9:g.9246601C>A	NCBI36
NG_012218.1:g.34152C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377403.7:c.1462C>A MANE Select	ENSP00000366620.2:p.Pro488Thr
ENST00000377403.6:c.1462C>A	ENSP00000366620.1:p.Pro488Thr
ENST00000602477.1:c.1495C>A	ENSP00000473348.1:p.Pro499Thr
NM_001282587.1:c.1495C>A	NP_001269516.1:p.Pro499Thr
NM_004285.3:c.1462C>A	NP_004276.2:p.Pro488Thr
XM_005263539.3:c.1495C>A	XP_005263596.1:p.Pro499Thr
XM_005263540.3:c.1489C>A	XP_005263597.1:p.Pro497Thr
XM_006711052.2:c.1462C>A	XP_006711115.1:p.Pro488Thr
XM_011542446.1:c.1462C>A	XP_011540748.1:p.Pro488Thr
XM_005263540.5:c.1489C>A	XP_005263597.1:p.Pro497Thr
XM_006711052.4:c.1462C>A	XP_006711115.1:p.Pro488Thr
XM_017002865.2:c.1462C>A	XP_016858354.1:p.Pro488Thr
XM_017002866.2:c.394C>A	XP_016858355.1:p.Pro132Thr
NM_001282587.2:c.1495C>A	NP_001269516.1:p.Pro499Thr
NM_004285.4:c.1462C>A MANE Select	NP_004276.2:p.Pro488Thr