Canonical Allele Identifier: CA7807634

Gene: GNPTG

Linked Data

• ClinVar Variation Id: 2920248
• ClinVar RCV Id: RCV003736198
• dbSNP Id: rs777991598
• ExAC: 16:1412029 G / C
• gnomAD v2: 16-1412029-G-C
• gnomAD v3: 16-1362028-G-C
• gnomAD v4: 16-1362028-G-C
• MyVariant Identifiers: chr16:g.1412029G>C (hg19) ; chr16:g.1362028G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362028G>C , CM000678.2:g.1362028G>C	GRCh38
NC_000016.9:g.1412029G>C , CM000678.1:g.1412029G>C	GRCh37
NC_000016.8:g.1352030G>C	NCBI36
NG_016985.1:g.15130G>C
NG_033129.1:g.57677C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.417-10G>C
ENST00000529110.2:c.402-10G>C	ENSP00000435349.2:n.402-10G>C
ENST00000529957.6:n.376-10G>C
ENST00000683366.1:c.*50-10G>C	ENSP00000507283.1:n.*50-10G>C
ENST00000683887.1:c.366-10G>C	ENSP00000506886.1:n.366-10G>C
ENST00000684100.1:n.312-10G>C
ENST00000684126.1:n.376-10G>C
ENST00000684688.1:n.943-10G>C
ENST00000204679.9:c.318-10G>C MANE Select	ENSP00000204679.4:n.318-10G>C
ENST00000204679.8:c.318-10G>C	ENSP00000204679.4:n.318-10G>C
ENST00000526820.5:c.*220-10G>C	ENSP00000434413.1:n.*220-10G>C
ENST00000527076.1:n.1334-10G>C
ENST00000527168.5:n.354-10G>C
ENST00000529110.1:c.385-10G>C
ENST00000529957.5:n.417-10G>C
NM_032520.4:c.318-10G>C	NP_115909.1:n.318-10G>C
XM_017023782.1:c.366-10G>C	XP_016879271.1:n.366-10G>C
XM_017023783.1:c.-43-10G>C	XP_016879272.1:n.-43-10G>C
NM_032520.5:c.318-10G>C MANE Select	NP_115909.1:n.318-10G>C