Canonical Allele Identifier: CA394188405

Gene: GNPTG

Linked Data

• MyVariant Identifiers: chr16:g.1412624T>G (hg19) ; chr16:g.1362623T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362623T>G , CM000678.2:g.1362623T>G	GRCh38
NC_000016.9:g.1412624T>G , CM000678.1:g.1412624T>G	GRCh37
NC_000016.8:g.1352625T>G	NCBI36
NG_016985.1:g.15725T>G
NG_033129.1:g.57082A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000527168.6:n.721T>G
ENST00000529110.2:c.706T>G	ENSP00000435349.2:p.Leu236Val
ENST00000529957.6:n.680T>G
ENST00000683366.1:c.*354T>G	ENSP00000507283.1:n.*354T>G
ENST00000683887.1:c.670T>G	ENSP00000506886.1:p.Leu224Val
ENST00000684100.1:n.616T>G
ENST00000684126.1:n.756T>G
ENST00000684688.1:n.1247T>G
ENST00000204679.9:c.622T>G MANE Select	ENSP00000204679.4:p.Leu208Val
ENST00000204679.8:c.622T>G	ENSP00000204679.4:p.Leu208Val
ENST00000527076.1:n.1845T>G
ENST00000527168.5:n.789T>G
ENST00000529957.5:n.721T>G
NM_032520.4:c.622T>G	NP_115909.1:p.Leu208Val
XM_017023782.1:c.670T>G	XP_016879271.1:p.Leu224Val
XM_017023783.1:c.262T>G	XP_016879272.1:p.Leu88Val
NM_032520.5:c.622T>G MANE Select	NP_115909.1:p.Leu208Val