Canonical Allele Identifier: CA394187231

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412062C>A (hg19) ; chr16:g.1362061C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362061C>A , CM000678.2:g.1362061C>A	GRCh38
NC_000016.9:g.1412062C>A , CM000678.1:g.1412062C>A	GRCh37
NC_000016.8:g.1352063C>A	NCBI36
NG_016985.1:g.15163C>A
NG_033129.1:g.57644G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.440C>A
ENST00000529110.2:c.425C>A	ENSP00000435349.2:p.Ala142Asp
ENST00000529957.6:n.399C>A
ENST00000683366.1:c.*73C>A	ENSP00000507283.1:n.*73C>A
ENST00000683887.1:c.389C>A	ENSP00000506886.1:p.Ala130Asp
ENST00000684100.1:n.335C>A
ENST00000684126.1:n.399C>A
ENST00000684688.1:n.966C>A
ENST00000204679.9:c.341C>A MANE Select	ENSP00000204679.4:p.Ala114Asp
ENST00000204679.8:c.341C>A	ENSP00000204679.4:p.Ala114Asp
ENST00000526820.5:c.*243C>A	ENSP00000434413.1:n.*243C>A
ENST00000527076.1:n.1357C>A
ENST00000527168.5:n.377C>A
ENST00000529110.1:c.408C>A
ENST00000529957.5:n.440C>A
NM_032520.4:c.341C>A	NP_115909.1:p.Ala114Asp
XM_017023782.1:c.389C>A	XP_016879271.1:p.Ala130Asp
XM_017023783.1:c.-20C>A	XP_016879272.1:n.-20C>A
NM_032520.5:c.341C>A MANE Select	NP_115909.1:p.Ala114Asp