Canonical Allele Identifier: CA382892778

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118895590T>G (hg19) ; chr11:g.119024880T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119024880T>G , CM000673.2:g.119024880T>G	GRCh38
NC_000011.9:g.118895590T>G , CM000673.1:g.118895590T>G	GRCh37
NC_000011.8:g.118400800T>G	NCBI36
NG_013331.1:g.11026A>C , LRG_187:g.11026A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1530A>C (SLC37A4)
ENST00000697845.1:n.2519A>C (SLC37A4)
ENST00000697846.1:n.1892A>C (SLC37A4)
ENST00000697847.1:n.1603A>C (SLC37A4)
ENST00000697849.1:n.3996A>C (SLC37A4)
ENST00000697850.1:n.2187A>C (SLC37A4)
ENST00000697851.1:n.3158A>C (SLC37A4)
ENST00000638186.1:n.1624A>C (SLC37A4)
ENST00000638360.1:n.1456A>C (SLC37A4)
ENST00000638925.1:n.1589A>C (SLC37A4)
ENST00000650539.1:n.1792A>C (SLC37A4)
ENST00000330775.9:c.*30A>C (SLC37A4)	ENSP00000476242.2:n.*30A>C
ENST00000357590.9:c.*30A>C (SLC37A4)	ENSP00000476176.2:n.*30A>C
ENST00000525102.5:n.2078A>C (SLC37A4)
ENST00000526275.5:n.2102A>C (SLC37A4)
ENST00000527992.5:n.1548A>C (SLC37A4)
ENST00000530407.5:n.1470A>C (SLC37A4)
ENST00000532085.1:n.5338A>C (SLC37A4)
ENST00000533058.5:c.605T>G (TRAPPC4)	ENSP00000432920.1:p.Val202Gly
ENST00000538950.5:c.*30A>C (SLC37A4)	ENSP00000475991.2:n.*30A>C
ENST00000545985.5:c.*30A>C (SLC37A4)	ENSP00000475241.2:n.*30A>C
NM_001164277.1:c.*30A>C , LRG_187t1:c.*30A>C (SLC37A4)	NP_001157749.1:n.*30A>C
NM_001164278.1:c.*30A>C (SLC37A4)	NP_001157750.1:n.*30A>C
NM_001164279.1:c.*30A>C (SLC37A4)	NP_001157751.1:n.*30A>C
NM_001164280.1:c.*30A>C (SLC37A4)	NP_001157752.1:n.*30A>C
NM_001467.5:c.*30A>C (SLC37A4)	NP_001458.1:n.*30A>C
NM_001164278.2:c.*30A>C (SLC37A4)	NP_001157750.1:n.*30A>C
NM_001164279.2:c.*30A>C (SLC37A4)	NP_001157751.1:n.*30A>C
NM_001164280.2:c.*30A>C (SLC37A4)	NP_001157752.1:n.*30A>C
NM_001467.6:c.*30A>C (SLC37A4)	NP_001458.1:n.*30A>C
NM_001164277.2:c.*30A>C (SLC37A4) MANE Select	NP_001157749.1:n.*30A>C