Canonical Allele Identifier: CA386293542

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102151363T>G (hg19) ; chr12:g.101757585T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101757585T>G , CM000674.2:g.101757585T>G	GRCh38
NC_000012.11:g.102151363T>G , CM000674.1:g.102151363T>G	GRCh37
NC_000012.10:g.100675494T>G	NCBI36
NG_021243.1:g.78283A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.3322A>C MANE Select	ENSP00000299314.7:p.Lys1108Gln
ENST00000299314.11:c.3322A>C	ENSP00000299314.7:p.Lys1108Gln
ENST00000549194.1:n.188A>C
ENST00000549738.5:c.73A>C	ENSP00000450161.1:p.Lys25Gln
ENST00000550718.1:c.134A>C
NM_024312.4:c.3322A>C	NP_077288.2:p.Lys1108Gln
XM_006719593.2:c.3322A>C	XP_006719656.1:p.Lys1108Gln
XM_011538731.1:c.3241A>C	XP_011537033.1:p.Lys1081Gln
XM_006719593.3:c.3322A>C	XP_006719656.1:p.Lys1108Gln
XM_011538731.2:c.3241A>C	XP_011537033.1:p.Lys1081Gln
XM_017019961.1:c.3106A>C	XP_016875450.1:p.Lys1036Gln
XM_017019962.2:c.2095A>C	XP_016875451.1:p.Lys699Gln
NM_024312.5:c.3322A>C MANE Select	NP_077288.2:p.Lys1108Gln