Canonical Allele Identifier: CA382894763

Gene: SLC37A4 TRAPPC4

Linked Data

• dbSNP Id: rs1157093654
• MyVariant Identifiers: chr11:g.118895768C>A (hg19) ; chr11:g.119025058C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025058C>A , CM000673.2:g.119025058C>A	GRCh38
NC_000011.9:g.118895768C>A , CM000673.1:g.118895768C>A	GRCh37
NC_000011.8:g.118400978C>A	NCBI36
NG_013331.1:g.10848G>T , LRG_187:g.10848G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1352G>T (SLC37A4)
ENST00000697845.1:n.2341G>T (SLC37A4)
ENST00000697846.1:n.1714G>T (SLC37A4)
ENST00000697847.1:n.1425G>T (SLC37A4)
ENST00000697849.1:n.3818G>T (SLC37A4)
ENST00000697850.1:n.2009G>T (SLC37A4)
ENST00000697851.1:n.2980G>T (SLC37A4)
ENST00000638186.1:n.1446G>T (SLC37A4)
ENST00000638360.1:n.1278G>T (SLC37A4)
ENST00000638925.1:n.1411G>T (SLC37A4)
ENST00000650539.1:n.1614G>T (SLC37A4)
ENST00000330775.9:c.1142G>T (SLC37A4)	ENSP00000476242.2:p.Gly381Val
ENST00000357590.9:c.1208G>T (SLC37A4)	ENSP00000476176.2:p.Gly403Val
ENST00000524428.5:n.1378G>T (SLC37A4)
ENST00000525039.5:n.1632G>T (SLC37A4)
ENST00000525102.5:n.1900G>T (SLC37A4)
ENST00000525372.5:n.1240G>T (SLC37A4)
ENST00000526275.5:n.1924G>T (SLC37A4)
ENST00000527992.5:n.1370G>T (SLC37A4)
ENST00000530407.5:n.1292G>T (SLC37A4)
ENST00000532085.1:n.5160G>T (SLC37A4)
ENST00000533058.5:c.*9C>A (TRAPPC4)	ENSP00000432920.1:n.*9C>A
ENST00000538950.5:c.923G>T (SLC37A4)	ENSP00000475991.2:p.Gly308Val
ENST00000545985.5:c.1142G>T (SLC37A4)	ENSP00000475241.2:p.Gly381Val
NM_001164277.1:c.1142G>T , LRG_187t1:c.1142G>T (SLC37A4)	NP_001157749.1:p.Gly381Val
NM_001164278.1:c.1208G>T (SLC37A4)	NP_001157750.1:p.Gly403Val
NM_001164279.1:c.923G>T (SLC37A4)	NP_001157751.1:p.Gly308Val
NM_001164280.1:c.1142G>T (SLC37A4)	NP_001157752.1:p.Gly381Val
NM_001467.5:c.1142G>T (SLC37A4)	NP_001458.1:p.Gly381Val
NM_001164278.2:c.1208G>T (SLC37A4)	NP_001157750.1:p.Gly403Val
NM_001164279.2:c.923G>T (SLC37A4)	NP_001157751.1:p.Gly308Val
NM_001164280.2:c.1142G>T (SLC37A4)	NP_001157752.1:p.Gly381Val
NM_001467.6:c.1142G>T (SLC37A4)	NP_001458.1:p.Gly381Val
NM_001164277.2:c.1142G>T (SLC37A4) MANE Select	NP_001157749.1:p.Gly381Val