Canonical Allele Identifier: CA394186858

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1411901A>C (hg19) ; chr16:g.1361900A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1361900A>C , CM000678.2:g.1361900A>C	GRCh38
NC_000016.9:g.1411901A>C , CM000678.1:g.1411901A>C	GRCh37
NC_000016.8:g.1351902A>C	NCBI36
NG_016985.1:g.15002A>C
NG_033129.1:g.57805T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.361A>C
ENST00000529110.2:c.346A>C	ENSP00000435349.2:p.Asn116His
ENST00000529957.6:n.320A>C
ENST00000683366.1:c.207A>C	ENSP00000507283.1:p.Thr69=
ENST00000683887.1:c.310A>C	ENSP00000506886.1:p.Asn104His
ENST00000684100.1:n.256A>C
ENST00000684126.1:n.320A>C
ENST00000684688.1:n.887A>C
ENST00000204679.9:c.262A>C MANE Select	ENSP00000204679.4:p.Asn88His
ENST00000204679.8:c.262A>C	ENSP00000204679.4:p.Asn88His
ENST00000526820.5:c.*164A>C	ENSP00000434413.1:n.*164A>C
ENST00000527076.1:n.1278A>C
ENST00000527168.5:n.298A>C
ENST00000529110.1:c.329A>C
ENST00000529957.5:n.361A>C
NM_032520.4:c.262A>C	NP_115909.1:p.Asn88His
XM_017023782.1:c.310A>C	XP_016879271.1:p.Asn104His
XM_017023783.1:c.-99A>C	XP_016879272.1:n.-99A>C
NM_032520.5:c.262A>C MANE Select	NP_115909.1:p.Asn88His