Canonical Allele Identifier: CA2201615216

Gene: GNPTG

Linked Data

• dbSNP Id: rs2034921930

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362557C>T , CM000678.2:g.1362557C>T	GRCh38
NC_000016.9:g.1412558C>T , CM000678.1:g.1412558C>T	GRCh37
NC_000016.8:g.1352559C>T	NCBI36
NG_016985.1:g.15659C>T
NG_033129.1:g.57148G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000527168.6:n.708+23C>T
ENST00000529110.2:c.693+23C>T	ENSP00000435349.2:n.693+23C>T
ENST00000529957.6:n.667+23C>T
ENST00000683366.1:c.*341+23C>T	ENSP00000507283.1:n.*341+23C>T
ENST00000683887.1:c.657+23C>T	ENSP00000506886.1:n.657+23C>T
ENST00000684100.1:n.603+23C>T
ENST00000684126.1:n.690C>T
ENST00000684688.1:n.1234+23C>T
ENST00000204679.9:c.609+23C>T MANE Select	ENSP00000204679.4:n.609+23C>T
ENST00000204679.8:c.609+23C>T	ENSP00000204679.4:n.609+23C>T
ENST00000527076.1:n.1779C>T
ENST00000527168.5:n.776+23C>T
ENST00000529957.5:n.708+23C>T
NM_032520.4:c.609+23C>T	NP_115909.1:n.609+23C>T
XM_017023782.1:c.657+23C>T	XP_016879271.1:n.657+23C>T
XM_017023783.1:c.249+23C>T	XP_016879272.1:n.249+23C>T
NM_032520.5:c.609+23C>T MANE Select	NP_115909.1:n.609+23C>T