Canonical Allele Identifier: CA2616339378

Gene: SLC37A4 TRAPPC4

Linked Data

• gnomAD v4: 11-119024697-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119024697A>G , CM000673.2:g.119024697A>G	GRCh38
NC_000011.9:g.118895407A>G , CM000673.1:g.118895407A>G	GRCh37
NC_000011.8:g.118400617A>G	NCBI36
NG_013331.1:g.11209T>C , LRG_187:g.11209T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1713T>C (SLC37A4)
ENST00000697845.1:n.2702T>C (SLC37A4)
ENST00000697846.1:n.2075T>C (SLC37A4)
ENST00000697847.1:n.1786T>C (SLC37A4)
ENST00000697849.1:n.4179T>C (SLC37A4)
ENST00000697850.1:n.2370T>C (SLC37A4)
ENST00000697851.1:n.3341T>C (SLC37A4)
ENST00000638186.1:n.1807T>C (SLC37A4)
ENST00000638360.1:n.1639T>C (SLC37A4)
ENST00000638925.1:n.1772T>C (SLC37A4)
ENST00000650539.1:n.1975T>C (SLC37A4)
ENST00000330775.9:c.*213T>C (SLC37A4)	ENSP00000476242.2:n.*213T>C
ENST00000357590.9:c.*213T>C (SLC37A4)	ENSP00000476176.2:n.*213T>C
ENST00000525102.5:n.2261T>C (SLC37A4)
ENST00000526275.5:n.2285T>C (SLC37A4)
ENST00000527992.5:n.1731T>C (SLC37A4)
ENST00000532085.1:n.5521T>C (SLC37A4)
ENST00000533058.5:c.582-160A>G (TRAPPC4)	ENSP00000432920.1:n.582-160A>G
ENST00000538950.5:c.*213T>C (SLC37A4)	ENSP00000475991.2:n.*213T>C
ENST00000545985.5:c.*213T>C (SLC37A4)	ENSP00000475241.2:n.*213T>C
NM_001164277.1:c.*213T>C , LRG_187t1:c.*213T>C (SLC37A4)	NP_001157749.1:n.*213T>C
NM_001164278.1:c.*213T>C (SLC37A4)	NP_001157750.1:n.*213T>C
NM_001164279.1:c.*213T>C (SLC37A4)	NP_001157751.1:n.*213T>C
NM_001164280.1:c.*213T>C (SLC37A4)	NP_001157752.1:n.*213T>C
NM_001467.5:c.*213T>C (SLC37A4)	NP_001458.1:n.*213T>C
NM_001164278.2:c.*213T>C (SLC37A4)	NP_001157750.1:n.*213T>C
NM_001164279.2:c.*213T>C (SLC37A4)	NP_001157751.1:n.*213T>C
NM_001164280.2:c.*213T>C (SLC37A4)	NP_001157752.1:n.*213T>C
NM_001467.6:c.*213T>C (SLC37A4)	NP_001458.1:n.*213T>C
NM_001164277.2:c.*213T>C (SLC37A4) MANE Select	NP_001157749.1:n.*213T>C