Canonical Allele Identifier: CA2616339318

Gene: SLC37A4 TRAPPC4

Linked Data

• gnomAD v4: 11-119024607-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119024607C>A , CM000673.2:g.119024607C>A	GRCh38
NC_000011.9:g.118895317C>A , CM000673.1:g.118895317C>A	GRCh37
NC_000011.8:g.118400527C>A	NCBI36
NG_013331.1:g.11299G>T , LRG_187:g.11299G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1803G>T (SLC37A4)
ENST00000697845.1:n.2792G>T (SLC37A4)
ENST00000697846.1:n.2165G>T (SLC37A4)
ENST00000697847.1:n.1876G>T (SLC37A4)
ENST00000697849.1:n.4269G>T (SLC37A4)
ENST00000697850.1:n.2460G>T (SLC37A4)
ENST00000697851.1:n.3431G>T (SLC37A4)
ENST00000638186.1:n.1897G>T (SLC37A4)
ENST00000638360.1:n.1729G>T (SLC37A4)
ENST00000638925.1:n.1862G>T (SLC37A4)
ENST00000650539.1:n.2065G>T (SLC37A4)
ENST00000330775.9:c.*303G>T (SLC37A4)	ENSP00000476242.2:n.*303G>T
ENST00000357590.9:c.*303G>T (SLC37A4)	ENSP00000476176.2:n.*303G>T
ENST00000525102.5:n.2351G>T (SLC37A4)
ENST00000526275.5:n.2375G>T (SLC37A4)
ENST00000527992.5:n.1821G>T (SLC37A4)
ENST00000532085.1:n.5611G>T (SLC37A4)
ENST00000533058.5:c.582-250C>A (TRAPPC4)	ENSP00000432920.1:n.582-250C>A
ENST00000538950.5:c.*303G>T (SLC37A4)	ENSP00000475991.2:n.*303G>T
ENST00000545985.5:c.*303G>T (SLC37A4)	ENSP00000475241.2:n.*303G>T
NM_001164277.1:c.*303G>T , LRG_187t1:c.*303G>T (SLC37A4)	NP_001157749.1:n.*303G>T
NM_001164278.1:c.*303G>T (SLC37A4)	NP_001157750.1:n.*303G>T
NM_001164279.1:c.*303G>T (SLC37A4)	NP_001157751.1:n.*303G>T
NM_001164280.1:c.*303G>T (SLC37A4)	NP_001157752.1:n.*303G>T
NM_001467.5:c.*303G>T (SLC37A4)	NP_001458.1:n.*303G>T
NM_001164278.2:c.*303G>T (SLC37A4)	NP_001157750.1:n.*303G>T
NM_001164279.2:c.*303G>T (SLC37A4)	NP_001157751.1:n.*303G>T
NM_001164280.2:c.*303G>T (SLC37A4)	NP_001157752.1:n.*303G>T
NM_001467.6:c.*303G>T (SLC37A4)	NP_001458.1:n.*303G>T
NM_001164277.2:c.*303G>T (SLC37A4) MANE Select	NP_001157749.1:n.*303G>T