Canonical Allele Identifier: CA394186920

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1411914A>C (hg19) ; chr16:g.1361913A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1361913A>C , CM000678.2:g.1361913A>C	GRCh38
NC_000016.9:g.1411914A>C , CM000678.1:g.1411914A>C	GRCh37
NC_000016.8:g.1351915A>C	NCBI36
NG_016985.1:g.15015A>C
NG_033129.1:g.57792T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.374A>C
ENST00000529110.2:c.359A>C	ENSP00000435349.2:p.His120Pro
ENST00000529957.6:n.333A>C
ENST00000683366.1:c.*7A>C	ENSP00000507283.1:n.*7A>C
ENST00000683887.1:c.323A>C	ENSP00000506886.1:p.His108Pro
ENST00000684100.1:n.269A>C
ENST00000684126.1:n.333A>C
ENST00000684688.1:n.900A>C
ENST00000204679.9:c.275A>C MANE Select	ENSP00000204679.4:p.His92Pro
ENST00000204679.8:c.275A>C	ENSP00000204679.4:p.His92Pro
ENST00000526820.5:c.*177A>C	ENSP00000434413.1:n.*177A>C
ENST00000527076.1:n.1291A>C
ENST00000527168.5:n.311A>C
ENST00000529110.1:c.342A>C
ENST00000529957.5:n.374A>C
NM_032520.4:c.275A>C	NP_115909.1:p.His92Pro
XM_017023782.1:c.323A>C	XP_016879271.1:p.His108Pro
XM_017023783.1:c.-86A>C	XP_016879272.1:n.-86A>C
NM_032520.5:c.275A>C MANE Select	NP_115909.1:p.His92Pro