Canonical Allele Identifier: CA382896103

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118895993C>G (hg19) ; chr11:g.119025283C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025283C>G , CM000673.2:g.119025283C>G	GRCh38
NC_000011.9:g.118895993C>G , CM000673.1:g.118895993C>G	GRCh37
NC_000011.8:g.118401203C>G	NCBI36
NG_013331.1:g.10623G>C , LRG_187:g.10623G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1241G>C (SLC37A4)
ENST00000697845.1:n.2230G>C (SLC37A4)
ENST00000697846.1:n.1603G>C (SLC37A4)
ENST00000697847.1:n.1314G>C (SLC37A4)
ENST00000697849.1:n.3707G>C (SLC37A4)
ENST00000697850.1:n.1898G>C (SLC37A4)
ENST00000697851.1:n.2869G>C (SLC37A4)
ENST00000638186.1:n.1335G>C (SLC37A4)
ENST00000638360.1:n.1167G>C (SLC37A4)
ENST00000638925.1:n.1300G>C (SLC37A4)
ENST00000650539.1:n.1503G>C (SLC37A4)
ENST00000330775.9:c.1031G>C (SLC37A4)	ENSP00000476242.2:p.Gly344Ala
ENST00000357590.9:c.1097G>C (SLC37A4)	ENSP00000476176.2:p.Gly366Ala
ENST00000524428.5:n.1267G>C (SLC37A4)
ENST00000525039.5:n.1521G>C (SLC37A4)
ENST00000525102.5:n.1789G>C (SLC37A4)
ENST00000525372.5:n.1129G>C (SLC37A4)
ENST00000526275.5:n.1813G>C (SLC37A4)
ENST00000527992.5:n.1259G>C (SLC37A4)
ENST00000529510.5:n.719G>C (SLC37A4)
ENST00000530407.5:n.1181G>C (SLC37A4)
ENST00000532085.1:n.5049G>C (SLC37A4)
ENST00000533058.5:c.*234C>G (TRAPPC4)	ENSP00000432920.1:n.*234C>G
ENST00000538950.5:c.812G>C (SLC37A4)	ENSP00000475991.2:p.Gly271Ala
ENST00000545985.5:c.1031G>C (SLC37A4)	ENSP00000475241.2:p.Gly344Ala
NM_001164277.1:c.1031G>C , LRG_187t1:c.1031G>C (SLC37A4)	NP_001157749.1:p.Gly344Ala
NM_001164278.1:c.1097G>C (SLC37A4)	NP_001157750.1:p.Gly366Ala
NM_001164279.1:c.812G>C (SLC37A4)	NP_001157751.1:p.Gly271Ala
NM_001164280.1:c.1031G>C (SLC37A4)	NP_001157752.1:p.Gly344Ala
NM_001467.5:c.1031G>C (SLC37A4)	NP_001458.1:p.Gly344Ala
NM_001164278.2:c.1097G>C (SLC37A4)	NP_001157750.1:p.Gly366Ala
NM_001164279.2:c.812G>C (SLC37A4)	NP_001157751.1:p.Gly271Ala
NM_001164280.2:c.1031G>C (SLC37A4)	NP_001157752.1:p.Gly344Ala
NM_001467.6:c.1031G>C (SLC37A4)	NP_001458.1:p.Gly344Ala
NM_001164277.2:c.1031G>C (SLC37A4) MANE Select	NP_001157749.1:p.Gly344Ala