Canonical Allele Identifier: CA386293669

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102151382G>C (hg19) ; chr12:g.101757604G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101757604G>C , CM000674.2:g.101757604G>C	GRCh38
NC_000012.11:g.102151382G>C , CM000674.1:g.102151382G>C	GRCh37
NC_000012.10:g.100675513G>C	NCBI36
NG_021243.1:g.78264C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.3303C>G MANE Select	ENSP00000299314.7:p.Ile1101Met
ENST00000299314.11:c.3303C>G	ENSP00000299314.7:p.Ile1101Met
ENST00000549194.1:n.169C>G
ENST00000549738.5:c.54C>G	ENSP00000450161.1:p.Ile18Met
ENST00000550718.1:c.115C>G
NM_024312.4:c.3303C>G	NP_077288.2:p.Ile1101Met
XM_006719593.2:c.3303C>G	XP_006719656.1:p.Ile1101Met
XM_011538731.1:c.3222C>G	XP_011537033.1:p.Ile1074Met
XM_006719593.3:c.3303C>G	XP_006719656.1:p.Ile1101Met
XM_011538731.2:c.3222C>G	XP_011537033.1:p.Ile1074Met
XM_017019961.1:c.3087C>G	XP_016875450.1:p.Ile1029Met
XM_017019962.2:c.2076C>G	XP_016875451.1:p.Ile692Met
NM_024312.5:c.3303C>G MANE Select	NP_077288.2:p.Ile1101Met