Canonical Allele Identifier: CA386294901

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102153903G>A (hg19) ; chr12:g.101760125G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101760125G>A , CM000674.2:g.101760125G>A	GRCh38
NC_000012.11:g.102153903G>A , CM000674.1:g.102153903G>A	GRCh37
NC_000012.10:g.100678034G>A	NCBI36
NG_021243.1:g.75743C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.3154C>T MANE Select	ENSP00000299314.7:p.His1052Tyr
ENST00000299314.11:c.3154C>T	ENSP00000299314.7:p.His1052Tyr
ENST00000549194.1:n.20C>T
NM_024312.4:c.3154C>T	NP_077288.2:p.His1052Tyr
XM_006719593.2:c.3154C>T	XP_006719656.1:p.His1052Tyr
XM_011538731.1:c.3073C>T	XP_011537033.1:p.His1025Tyr
XM_006719593.3:c.3154C>T	XP_006719656.1:p.His1052Tyr
XM_011538731.2:c.3073C>T	XP_011537033.1:p.His1025Tyr
XM_017019961.1:c.2938C>T	XP_016875450.1:p.His980Tyr
XM_017019962.2:c.1927C>T	XP_016875451.1:p.His643Tyr
NM_024312.5:c.3154C>T MANE Select	NP_077288.2:p.His1052Tyr