Canonical Allele Identifier: CA2616339446

Gene: SLC37A4 TRAPPC4

Linked Data

• gnomAD v4: 11-119024767-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119024767C>A , CM000673.2:g.119024767C>A	GRCh38
NC_000011.9:g.118895477C>A , CM000673.1:g.118895477C>A	GRCh37
NC_000011.8:g.118400687C>A	NCBI36
NG_013331.1:g.11139G>T , LRG_187:g.11139G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1643G>T (SLC37A4)
ENST00000697845.1:n.2632G>T (SLC37A4)
ENST00000697846.1:n.2005G>T (SLC37A4)
ENST00000697847.1:n.1716G>T (SLC37A4)
ENST00000697849.1:n.4109G>T (SLC37A4)
ENST00000697850.1:n.2300G>T (SLC37A4)
ENST00000697851.1:n.3271G>T (SLC37A4)
ENST00000638186.1:n.1737G>T (SLC37A4)
ENST00000638360.1:n.1569G>T (SLC37A4)
ENST00000638925.1:n.1702G>T (SLC37A4)
ENST00000650539.1:n.1905G>T (SLC37A4)
ENST00000330775.9:c.*143G>T (SLC37A4)	ENSP00000476242.2:n.*143G>T
ENST00000357590.9:c.*143G>T (SLC37A4)	ENSP00000476176.2:n.*143G>T
ENST00000525102.5:n.2191G>T (SLC37A4)
ENST00000526275.5:n.2215G>T (SLC37A4)
ENST00000527992.5:n.1661G>T (SLC37A4)
ENST00000532085.1:n.5451G>T (SLC37A4)
ENST00000533058.5:c.582-90C>A (TRAPPC4)	ENSP00000432920.1:n.582-90C>A
ENST00000538950.5:c.*143G>T (SLC37A4)	ENSP00000475991.2:n.*143G>T
ENST00000545985.5:c.*143G>T (SLC37A4)	ENSP00000475241.2:n.*143G>T
NM_001164277.1:c.*143G>T , LRG_187t1:c.*143G>T (SLC37A4)	NP_001157749.1:n.*143G>T
NM_001164278.1:c.*143G>T (SLC37A4)	NP_001157750.1:n.*143G>T
NM_001164279.1:c.*143G>T (SLC37A4)	NP_001157751.1:n.*143G>T
NM_001164280.1:c.*143G>T (SLC37A4)	NP_001157752.1:n.*143G>T
NM_001467.5:c.*143G>T (SLC37A4)	NP_001458.1:n.*143G>T
NM_001164278.2:c.*143G>T (SLC37A4)	NP_001157750.1:n.*143G>T
NM_001164279.2:c.*143G>T (SLC37A4)	NP_001157751.1:n.*143G>T
NM_001164280.2:c.*143G>T (SLC37A4)	NP_001157752.1:n.*143G>T
NM_001467.6:c.*143G>T (SLC37A4)	NP_001458.1:n.*143G>T
NM_001164277.2:c.*143G>T (SLC37A4) MANE Select	NP_001157749.1:n.*143G>T