Canonical Allele Identifier: CA412896507

Gene: SLC35A2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48906433G>A , CM000685.2:g.48906433G>A	GRCh38
NC_000023.10:g.48763710G>A , CM000685.1:g.48763710G>A	GRCh37
NC_000023.9:g.48648654G>A	NCBI36
NG_034300.1:g.10526C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005660.3:c.385C>T MANE Select	NP_005651.1:p.Gln129Ter
ENST00000247138.11:c.385C>T MANE Select	ENSP00000247138.5:p.Gln129Ter
NM_001032289.2:c.385C>T	NP_001027460.1:p.Gln129Ter
NM_001032289.3:c.385C>T	NP_001027460.1:p.Gln129Ter
NM_001042498.2:c.385C>T	NP_001035963.1:p.Gln129Ter
NM_001042498.3:c.385C>T	NP_001035963.1:p.Gln129Ter
NM_001282647.1:c.385C>T	NP_001269576.1:p.Gln129Ter
NM_001282647.2:c.385C>T	NP_001269576.1:p.Gln129Ter
NM_001282648.1:c.313C>T	NP_001269577.1:p.Gln105Ter
NM_001282648.2:c.313C>T	NP_001269577.1:p.Gln105Ter
NM_001282649.1:c.202C>T	NP_001269578.1:p.Gln68Ter
NM_001282649.2:c.202C>T	NP_001269578.1:p.Gln68Ter
NM_001282650.1:c.424C>T	NP_001269579.1:p.Gln142Ter
NM_001282650.2:c.424C>T	NP_001269579.1:p.Gln142Ter
NM_001282651.1:c.469C>T	NP_001269580.1:p.Gln157Ter
NM_001282651.2:c.469C>T	NP_001269580.1:p.Gln157Ter
NM_005660.2:c.385C>T	NP_005651.1:p.Gln129Ter
ENST00000247138.10:c.385C>T	ENSP00000247138.5:p.Gln129Ter
ENST00000376512.2:c.385C>T	ENSP00000365695.1:p.Gln129Ter
ENST00000376515.8:c.313C>T	ENSP00000365698.3:p.Gln105Ter
ENST00000376521.6:c.385C>T	ENSP00000365704.1:p.Gln129Ter
ENST00000376529.8:c.385C>T	ENSP00000365712.3:p.Gln129Ter
ENST00000413561.7:c.170C>T
ENST00000445167.7:c.385C>T	ENSP00000402726.2:p.Gln129Ter
ENST00000446885.1:c.169C>T	ENSP00000415518.1:p.Gln57Ter
ENST00000452555.7:c.469C>T	ENSP00000416002.2:p.Gln157Ter
ENST00000616181.5:c.424C>T	ENSP00000478617.1:p.Gln142Ter
ENST00000634461.1:c.202C>T	ENSP00000489440.1:p.Gln68Ter
ENST00000634665.1:c.*5C>T	ENSP00000489356.1:n.*5C>T
ENST00000635015.1:c.424C>T	ENSP00000489089.1:p.Gln142Ter
ENST00000635238.1:c.346C>T	ENSP00000489515.1:p.Gln116Ter
ENST00000635285.1:c.385C>T	ENSP00000489484.1:p.Gln129Ter
ENST00000635460.1:c.383C>T
ENST00000635589.1:c.202C>T	ENSP00000489197.1:p.Gln68Ter
ENST00000635628.1:c.*279C>T	ENSP00000489613.1:n.*279C>T