Canonical Allele Identifier: CA382892549

Gene: SLC37A4 TRAPPC4

Linked Data

• gnomAD v4: 11-119024864-A-G
• MyVariant Identifiers: chr11:g.118895574A>G (hg19) ; chr11:g.119024864A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119024864A>G , CM000673.2:g.119024864A>G	GRCh38
NC_000011.9:g.118895574A>G , CM000673.1:g.118895574A>G	GRCh37
NC_000011.8:g.118400784A>G	NCBI36
NG_013331.1:g.11042T>C , LRG_187:g.11042T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1546T>C (SLC37A4)
ENST00000697845.1:n.2535T>C (SLC37A4)
ENST00000697846.1:n.1908T>C (SLC37A4)
ENST00000697847.1:n.1619T>C (SLC37A4)
ENST00000697849.1:n.4012T>C (SLC37A4)
ENST00000697850.1:n.2203T>C (SLC37A4)
ENST00000697851.1:n.3174T>C (SLC37A4)
ENST00000638186.1:n.1640T>C (SLC37A4)
ENST00000638360.1:n.1472T>C (SLC37A4)
ENST00000638925.1:n.1605T>C (SLC37A4)
ENST00000650539.1:n.1808T>C (SLC37A4)
ENST00000330775.9:c.*46T>C (SLC37A4)	ENSP00000476242.2:n.*46T>C
ENST00000357590.9:c.*46T>C (SLC37A4)	ENSP00000476176.2:n.*46T>C
ENST00000525102.5:n.2094T>C (SLC37A4)
ENST00000526275.5:n.2118T>C (SLC37A4)
ENST00000527992.5:n.1564T>C (SLC37A4)
ENST00000532085.1:n.5354T>C (SLC37A4)
ENST00000533058.5:c.589A>G (TRAPPC4)	ENSP00000432920.1:p.Arg197Gly
ENST00000538950.5:c.*46T>C (SLC37A4)	ENSP00000475991.2:n.*46T>C
ENST00000545985.5:c.*46T>C (SLC37A4)	ENSP00000475241.2:n.*46T>C
NM_001164277.1:c.*46T>C , LRG_187t1:c.*46T>C (SLC37A4)	NP_001157749.1:n.*46T>C
NM_001164278.1:c.*46T>C (SLC37A4)	NP_001157750.1:n.*46T>C
NM_001164279.1:c.*46T>C (SLC37A4)	NP_001157751.1:n.*46T>C
NM_001164280.1:c.*46T>C (SLC37A4)	NP_001157752.1:n.*46T>C
NM_001467.5:c.*46T>C (SLC37A4)	NP_001458.1:n.*46T>C
NM_001164278.2:c.*46T>C (SLC37A4)	NP_001157750.1:n.*46T>C
NM_001164279.2:c.*46T>C (SLC37A4)	NP_001157751.1:n.*46T>C
NM_001164280.2:c.*46T>C (SLC37A4)	NP_001157752.1:n.*46T>C
NM_001467.6:c.*46T>C (SLC37A4)	NP_001458.1:n.*46T>C
NM_001164277.2:c.*46T>C (SLC37A4) MANE Select	NP_001157749.1:n.*46T>C