Canonical Allele Identifier: CA6311565

Gene: SLC37A4 TRAPPC4

Linked Data

• dbSNP Id: rs782276923
• ExAC: 11:118895588 C / A
• gnomAD v2: 11-118895588-C-A
• gnomAD v4: 11-119024878-C-A
• MyVariant Identifiers: chr11:g.118895588C>A (hg19) ; chr11:g.119024878C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119024878C>A , CM000673.2:g.119024878C>A	GRCh38
NC_000011.9:g.118895588C>A , CM000673.1:g.118895588C>A	GRCh37
NC_000011.8:g.118400798C>A	NCBI36
NG_013331.1:g.11028G>T , LRG_187:g.11028G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1532G>T (SLC37A4)
ENST00000697845.1:n.2521G>T (SLC37A4)
ENST00000697846.1:n.1894G>T (SLC37A4)
ENST00000697847.1:n.1605G>T (SLC37A4)
ENST00000697849.1:n.3998G>T (SLC37A4)
ENST00000697850.1:n.2189G>T (SLC37A4)
ENST00000697851.1:n.3160G>T (SLC37A4)
ENST00000638186.1:n.1626G>T (SLC37A4)
ENST00000638360.1:n.1458G>T (SLC37A4)
ENST00000638925.1:n.1591G>T (SLC37A4)
ENST00000650539.1:n.1794G>T (SLC37A4)
ENST00000330775.9:c.*32G>T (SLC37A4)	ENSP00000476242.2:n.*32G>T
ENST00000357590.9:c.*32G>T (SLC37A4)	ENSP00000476176.2:n.*32G>T
ENST00000525102.5:n.2080G>T (SLC37A4)
ENST00000526275.5:n.2104G>T (SLC37A4)
ENST00000527992.5:n.1550G>T (SLC37A4)
ENST00000530407.5:n.1472G>T (SLC37A4)
ENST00000532085.1:n.5340G>T (SLC37A4)
ENST00000533058.5:c.603C>A (TRAPPC4)	ENSP00000432920.1:p.Thr201=
ENST00000538950.5:c.*32G>T (SLC37A4)	ENSP00000475991.2:n.*32G>T
ENST00000545985.5:c.*32G>T (SLC37A4)	ENSP00000475241.2:n.*32G>T
NM_001164277.1:c.*32G>T , LRG_187t1:c.*32G>T (SLC37A4)	NP_001157749.1:n.*32G>T
NM_001164278.1:c.*32G>T (SLC37A4)	NP_001157750.1:n.*32G>T
NM_001164279.1:c.*32G>T (SLC37A4)	NP_001157751.1:n.*32G>T
NM_001164280.1:c.*32G>T (SLC37A4)	NP_001157752.1:n.*32G>T
NM_001467.5:c.*32G>T (SLC37A4)	NP_001458.1:n.*32G>T
NM_001164278.2:c.*32G>T (SLC37A4)	NP_001157750.1:n.*32G>T
NM_001164279.2:c.*32G>T (SLC37A4)	NP_001157751.1:n.*32G>T
NM_001164280.2:c.*32G>T (SLC37A4)	NP_001157752.1:n.*32G>T
NM_001467.6:c.*32G>T (SLC37A4)	NP_001458.1:n.*32G>T
NM_001164277.2:c.*32G>T (SLC37A4) MANE Select	NP_001157749.1:n.*32G>T