Canonical Allele Identifier: CA386304876

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102179841T>G (hg19) ; chr12:g.101786063T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101786063T>G , CM000674.2:g.101786063T>G	GRCh38
NC_000012.11:g.102179841T>G , CM000674.1:g.102179841T>G	GRCh37
NC_000012.10:g.100703972T>G	NCBI36
NG_021243.1:g.49805A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.520A>C MANE Select	ENSP00000299314.7:p.Lys174Gln
ENST00000299314.11:c.520A>C	ENSP00000299314.7:p.Lys174Gln
ENST00000549940.5:c.520A>C	ENSP00000449150.1:p.Lys174Gln
ENST00000550352.1:n.314A>C
ENST00000552681.1:c.154A>C	ENSP00000449217.1:p.Lys52Gln
NM_024312.4:c.520A>C	NP_077288.2:p.Lys174Gln
XM_006719593.2:c.520A>C	XP_006719656.1:p.Lys174Gln
XM_011538731.1:c.439A>C	XP_011537033.1:p.Lys147Gln
XM_006719593.3:c.520A>C	XP_006719656.1:p.Lys174Gln
XM_011538731.2:c.439A>C	XP_011537033.1:p.Lys147Gln
XM_017019961.1:c.304A>C	XP_016875450.1:p.Lys102Gln
XM_017019962.2:c.-831A>C	XP_016875451.1:n.-831A>C
NM_024312.5:c.520A>C MANE Select	NP_077288.2:p.Lys174Gln