Canonical Allele Identifier: CA481318576

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102153907C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101760129C>G , CM000674.2:g.101760129C>G	GRCh38
NC_000012.11:g.102153907C>G , CM000674.1:g.102153907C>G	GRCh37
NC_000012.10:g.100678038C>G	NCBI36
NG_021243.1:g.75739G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.3150G>C MANE Select	ENSP00000299314.7:p.Leu1050=
ENST00000299314.11:c.3150G>C	ENSP00000299314.7:p.Leu1050=
ENST00000549194.1:n.16G>C
NM_024312.4:c.3150G>C	NP_077288.2:p.Leu1050=
XM_006719593.2:c.3150G>C	XP_006719656.1:p.Leu1050=
XM_011538731.1:c.3069G>C	XP_011537033.1:p.Leu1023=
XM_006719593.3:c.3150G>C	XP_006719656.1:p.Leu1050=
XM_011538731.2:c.3069G>C	XP_011537033.1:p.Leu1023=
XM_017019961.1:c.2934G>C	XP_016875450.1:p.Leu978=
XM_017019962.2:c.1923G>C	XP_016875451.1:p.Leu641=
NM_024312.5:c.3150G>C MANE Select	NP_077288.2:p.Leu1050=