Canonical Allele Identifier: CA386294583

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102153812T>G (hg19) ; chr12:g.101760034T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101760034T>G , CM000674.2:g.101760034T>G	GRCh38
NC_000012.11:g.102153812T>G , CM000674.1:g.102153812T>G	GRCh37
NC_000012.10:g.100677943T>G	NCBI36
NG_021243.1:g.75834A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.3245A>C MANE Select	ENSP00000299314.7:p.Asn1082Thr
ENST00000299314.11:c.3245A>C	ENSP00000299314.7:p.Asn1082Thr
ENST00000549194.1:n.111A>C
ENST00000550718.1:c.57A>C
NM_024312.4:c.3245A>C	NP_077288.2:p.Asn1082Thr
XM_006719593.2:c.3245A>C	XP_006719656.1:p.Asn1082Thr
XM_011538731.1:c.3164A>C	XP_011537033.1:p.Asn1055Thr
XM_006719593.3:c.3245A>C	XP_006719656.1:p.Asn1082Thr
XM_011538731.2:c.3164A>C	XP_011537033.1:p.Asn1055Thr
XM_017019961.1:c.3029A>C	XP_016875450.1:p.Asn1010Thr
XM_017019962.2:c.2018A>C	XP_016875451.1:p.Asn673Thr
NM_024312.5:c.3245A>C MANE Select	NP_077288.2:p.Asn1082Thr