Canonical Allele Identifier: CA386305802

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102190526C>G (hg19) ; chr12:g.101796748C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101796748C>G , CM000674.2:g.101796748C>G	GRCh38
NC_000012.11:g.102190526C>G , CM000674.1:g.102190526C>G	GRCh37
NC_000012.10:g.100714657C>G	NCBI36
NG_021243.1:g.39120G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.132G>C MANE Select	ENSP00000299314.7:p.Trp44Cys
ENST00000647144.1:n.252G>C
ENST00000299314.11:c.132G>C	ENSP00000299314.7:p.Trp44Cys
ENST00000392919.4:c.132G>C	ENSP00000376651.4:p.Trp44Cys
ENST00000549165.1:c.132G>C	ENSP00000450413.1:p.Trp44Cys
ENST00000549940.5:c.132G>C	ENSP00000449150.1:p.Trp44Cys
NM_024312.4:c.132G>C	NP_077288.2:p.Trp44Cys
XM_006719593.2:c.132G>C	XP_006719656.1:p.Trp44Cys
XM_011538731.1:c.51G>C	XP_011537033.1:p.Trp17Cys
XM_006719593.3:c.132G>C	XP_006719656.1:p.Trp44Cys
XM_011538731.2:c.51G>C	XP_011537033.1:p.Trp17Cys
XM_017019961.1:c.-85G>C	XP_016875450.1:n.-85G>C
XM_017019962.2:c.-1219G>C	XP_016875451.1:n.-1219G>C
NM_024312.5:c.132G>C MANE Select	NP_077288.2:p.Trp44Cys