Canonical Allele Identifier: CA2616339394

Gene: SLC37A4 TRAPPC4

Linked Data

• gnomAD v4: 11-119024719-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119024719T>G , CM000673.2:g.119024719T>G	GRCh38
NC_000011.9:g.118895429T>G , CM000673.1:g.118895429T>G	GRCh37
NC_000011.8:g.118400639T>G	NCBI36
NG_013331.1:g.11187A>C , LRG_187:g.11187A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1691A>C (SLC37A4)
ENST00000697845.1:n.2680A>C (SLC37A4)
ENST00000697846.1:n.2053A>C (SLC37A4)
ENST00000697847.1:n.1764A>C (SLC37A4)
ENST00000697849.1:n.4157A>C (SLC37A4)
ENST00000697850.1:n.2348A>C (SLC37A4)
ENST00000697851.1:n.3319A>C (SLC37A4)
ENST00000638186.1:n.1785A>C (SLC37A4)
ENST00000638360.1:n.1617A>C (SLC37A4)
ENST00000638925.1:n.1750A>C (SLC37A4)
ENST00000650539.1:n.1953A>C (SLC37A4)
ENST00000330775.9:c.*191A>C (SLC37A4)	ENSP00000476242.2:n.*191A>C
ENST00000357590.9:c.*191A>C (SLC37A4)	ENSP00000476176.2:n.*191A>C
ENST00000525102.5:n.2239A>C (SLC37A4)
ENST00000526275.5:n.2263A>C (SLC37A4)
ENST00000527992.5:n.1709A>C (SLC37A4)
ENST00000532085.1:n.5499A>C (SLC37A4)
ENST00000533058.5:c.582-138T>G (TRAPPC4)	ENSP00000432920.1:n.582-138T>G
ENST00000538950.5:c.*191A>C (SLC37A4)	ENSP00000475991.2:n.*191A>C
ENST00000545985.5:c.*191A>C (SLC37A4)	ENSP00000475241.2:n.*191A>C
NM_001164277.1:c.*191A>C , LRG_187t1:c.*191A>C (SLC37A4)	NP_001157749.1:n.*191A>C
NM_001164278.1:c.*191A>C (SLC37A4)	NP_001157750.1:n.*191A>C
NM_001164279.1:c.*191A>C (SLC37A4)	NP_001157751.1:n.*191A>C
NM_001164280.1:c.*191A>C (SLC37A4)	NP_001157752.1:n.*191A>C
NM_001467.5:c.*191A>C (SLC37A4)	NP_001458.1:n.*191A>C
NM_001164278.2:c.*191A>C (SLC37A4)	NP_001157750.1:n.*191A>C
NM_001164279.2:c.*191A>C (SLC37A4)	NP_001157751.1:n.*191A>C
NM_001164280.2:c.*191A>C (SLC37A4)	NP_001157752.1:n.*191A>C
NM_001467.6:c.*191A>C (SLC37A4)	NP_001458.1:n.*191A>C
NM_001164277.2:c.*191A>C (SLC37A4) MANE Select	NP_001157749.1:n.*191A>C