Canonical Allele Identifier: CA2201613962

Gene: GNPTG

Linked Data

• dbSNP Id: rs2034888161

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1361840_1361846dup , CM000678.2:g.1361840_1361846dup	GRCh38
NC_000016.9:g.1411841_1411847dup , CM000678.1:g.1411841_1411847dup	GRCh37
NC_000016.8:g.1351842_1351848dup	NCBI36
NG_016985.1:g.14942_14948dup
NG_033129.1:g.57859_57865dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.333-32_333-26dup
ENST00000529110.2:c.318-32_318-26dup	ENSP00000435349.2:n.318-32_318-26dup
ENST00000529957.6:n.292-32_292-26dup
ENST00000683366.1:c.179-32_179-26dup	ENSP00000507283.1:n.179-32_179-26dup
ENST00000683887.1:c.282-32_282-26dup	ENSP00000506886.1:n.282-32_282-26dup
ENST00000684100.1:n.196_202dup
ENST00000684126.1:n.292-32_292-26dup
ENST00000684688.1:n.859-32_859-26dup
ENST00000204679.9:c.234-32_234-26dup MANE Select	ENSP00000204679.4:n.234-32_234-26dup
ENST00000204679.8:c.234-32_234-26dup	ENSP00000204679.4:n.234-32_234-26dup
ENST00000526820.5:c.*136-32_*136-26dup	ENSP00000434413.1:n.*136-32_*136-26dup
ENST00000527076.1:n.1218_1224dup
ENST00000527168.5:n.270-32_270-26dup
ENST00000529110.1:c.301-32_301-26dup
ENST00000529957.5:n.333-32_333-26dup
NM_032520.4:c.234-32_234-26dup	NP_115909.1:n.234-32_234-26dup
XM_017023782.1:c.282-32_282-26dup	XP_016879271.1:n.282-32_282-26dup
XM_017023783.1:c.-127-32_-127-26dup	XP_016879272.1:n.-127-32_-127-26dup
NM_032520.5:c.234-32_234-26dup MANE Select	NP_115909.1:n.234-32_234-26dup