Canonical Allele Identifier: CA386304873

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102179839T>G (hg19) ; chr12:g.101786061T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101786061T>G , CM000674.2:g.101786061T>G	GRCh38
NC_000012.11:g.102179839T>G , CM000674.1:g.102179839T>G	GRCh37
NC_000012.10:g.100703970T>G	NCBI36
NG_021243.1:g.49807A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.522A>C MANE Select	ENSP00000299314.7:p.Lys174Asn
ENST00000299314.11:c.522A>C	ENSP00000299314.7:p.Lys174Asn
ENST00000549940.5:c.522A>C	ENSP00000449150.1:p.Lys174Asn
ENST00000550352.1:n.316A>C
ENST00000552681.1:c.156A>C	ENSP00000449217.1:p.Lys52Asn
NM_024312.4:c.522A>C	NP_077288.2:p.Lys174Asn
XM_006719593.2:c.522A>C	XP_006719656.1:p.Lys174Asn
XM_011538731.1:c.441A>C	XP_011537033.1:p.Lys147Asn
XM_006719593.3:c.522A>C	XP_006719656.1:p.Lys174Asn
XM_011538731.2:c.441A>C	XP_011537033.1:p.Lys147Asn
XM_017019961.1:c.306A>C	XP_016875450.1:p.Lys102Asn
XM_017019962.2:c.-829A>C	XP_016875451.1:n.-829A>C
NM_024312.5:c.522A>C MANE Select	NP_077288.2:p.Lys174Asn