Canonical Allele Identifier: CA394187086

Gene: GNPTG

Linked Data

• gnomAD v4: 16-1361955-G-T
• MyVariant Identifiers: chr16:g.1411956G>T (hg19) ; chr16:g.1361955G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1361955G>T , CM000678.2:g.1361955G>T	GRCh38
NC_000016.9:g.1411956G>T , CM000678.1:g.1411956G>T	GRCh37
NC_000016.8:g.1351957G>T	NCBI36
NG_016985.1:g.15057G>T
NG_033129.1:g.57750C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.416G>T
ENST00000529110.2:c.401G>T	ENSP00000435349.2:p.Gly134Val
ENST00000529957.6:n.375G>T
ENST00000683366.1:c.*49G>T	ENSP00000507283.1:n.*49G>T
ENST00000683887.1:c.365G>T	ENSP00000506886.1:p.Gly122Val
ENST00000684100.1:n.311G>T
ENST00000684126.1:n.375G>T
ENST00000684688.1:n.942G>T
ENST00000204679.9:c.317G>T MANE Select	ENSP00000204679.4:p.Gly106Val
ENST00000204679.8:c.317G>T	ENSP00000204679.4:p.Gly106Val
ENST00000526820.5:c.*219G>T	ENSP00000434413.1:n.*219G>T
ENST00000527076.1:n.1333G>T
ENST00000527168.5:n.353G>T
ENST00000529110.1:c.384G>T
ENST00000529957.5:n.416G>T
NM_032520.4:c.317G>T	NP_115909.1:p.Gly106Val
XM_017023782.1:c.365G>T	XP_016879271.1:p.Gly122Val
XM_017023783.1:c.-44G>T	XP_016879272.1:n.-44G>T
NM_032520.5:c.317G>T MANE Select	NP_115909.1:p.Gly106Val