Canonical Allele Identifier: CA394187562

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412205A>C (hg19) ; chr16:g.1362204A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362204A>C , CM000678.2:g.1362204A>C	GRCh38
NC_000016.9:g.1412205A>C , CM000678.1:g.1412205A>C	GRCh37
NC_000016.8:g.1352206A>C	NCBI36
NG_016985.1:g.15306A>C
NG_033129.1:g.57501T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.511-2A>C
ENST00000529110.2:c.496-2A>C	ENSP00000435349.2:n.496-2A>C
ENST00000529957.6:n.470-2A>C
ENST00000683366.1:c.*144-2A>C	ENSP00000507283.1:n.*144-2A>C
ENST00000683887.1:c.460-2A>C	ENSP00000506886.1:n.460-2A>C
ENST00000684100.1:n.406-2A>C
ENST00000684126.1:n.470-2A>C
ENST00000684688.1:n.1037-2A>C
ENST00000204679.9:c.412-2A>C MANE Select	ENSP00000204679.4:n.412-2A>C
ENST00000204679.8:c.412-2A>C	ENSP00000204679.4:n.412-2A>C
ENST00000527076.1:n.1428-2A>C
ENST00000527168.5:n.448-2A>C
ENST00000529110.1:c.479-2A>C
ENST00000529957.5:n.511-2A>C
NM_032520.4:c.412-2A>C	NP_115909.1:n.412-2A>C
XM_017023782.1:c.460-2A>C	XP_016879271.1:n.460-2A>C
XM_017023783.1:c.52-2A>C	XP_016879272.1:n.52-2A>C
NM_032520.5:c.412-2A>C MANE Select	NP_115909.1:n.412-2A>C