Canonical Allele Identifier: CA7807772

Gene: GNPTG

Linked Data

• dbSNP Id: rs76695056
• ExAC: 16:1412362 G / C
• gnomAD v2: 16-1412362-G-C
• gnomAD v3: 16-1362361-G-C
• gnomAD v4: 16-1362361-G-C
• MyVariant Identifiers: chr16:g.1412362G>C (hg19) ; chr16:g.1362361G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362361G>C , CM000678.2:g.1362361G>C	GRCh38
NC_000016.9:g.1412362G>C , CM000678.1:g.1412362G>C	GRCh37
NC_000016.8:g.1352363G>C	NCBI36
NG_016985.1:g.15463G>C
NG_033129.1:g.57344C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.625+41G>C
ENST00000529110.2:c.610+41G>C	ENSP00000435349.2:n.610+41G>C
ENST00000529957.6:n.584+41G>C
ENST00000683366.1:c.*258+41G>C	ENSP00000507283.1:n.*258+41G>C
ENST00000683887.1:c.574+41G>C	ENSP00000506886.1:n.574+41G>C
ENST00000684100.1:n.520+41G>C
ENST00000684126.1:n.584+41G>C
ENST00000684688.1:n.1151+41G>C
ENST00000204679.9:c.526+41G>C MANE Select	ENSP00000204679.4:n.526+41G>C
ENST00000204679.8:c.526+41G>C	ENSP00000204679.4:n.526+41G>C
ENST00000527076.1:n.1583G>C
ENST00000527168.5:n.603G>C
ENST00000529957.5:n.625+41G>C
NM_032520.4:c.526+41G>C	NP_115909.1:n.526+41G>C
XM_017023782.1:c.574+41G>C	XP_016879271.1:n.574+41G>C
XM_017023783.1:c.166+41G>C	XP_016879272.1:n.166+41G>C
NM_032520.5:c.526+41G>C MANE Select	NP_115909.1:n.526+41G>C