Canonical Allele Identifier: CA2573146960
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1475687
ClinVar RCV Id: RCV002007929
dbSNP Id: rs2134627689

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025186C>T , CM000673.2:g.119025186C>T GRCh38
NC_000011.9:g.118895896C>T , CM000673.1:g.118895896C>T GRCh37
NC_000011.8:g.118401106C>T NCBI36
NG_013331.1:g.10720G>A , LRG_187:g.10720G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.1333+5G>A (SLC37A4)
ENST00000697845.1:n.2322+5G>A (SLC37A4)
ENST00000697846.1:n.1695+5G>A (SLC37A4)
ENST00000697847.1:n.1406+5G>A (SLC37A4)
ENST00000697849.1:n.3799+5G>A (SLC37A4)
ENST00000697850.1:n.1990+5G>A (SLC37A4)
ENST00000697851.1:n.2961+5G>A (SLC37A4)
ENST00000638186.1:n.1427+5G>A (SLC37A4)
ENST00000638360.1:n.1259+5G>A (SLC37A4)
ENST00000638925.1:n.1392+5G>A (SLC37A4)
ENST00000650539.1:n.1595+5G>A (SLC37A4)
ENST00000330775.9:c.1123+5G>A (SLC37A4) ENSP00000476242.2:n.1123+5G>A
ENST00000357590.9:c.1189+5G>A (SLC37A4) ENSP00000476176.2:n.1189+5G>A
ENST00000524428.5:n.1359+5G>A (SLC37A4)
ENST00000525039.5:n.1613+5G>A (SLC37A4)
ENST00000525102.5:n.1881+5G>A (SLC37A4)
ENST00000525372.5:n.1221+5G>A (SLC37A4)
ENST00000526275.5:n.1905+5G>A (SLC37A4)
ENST00000527992.5:n.1351+5G>A (SLC37A4)
ENST00000529510.5:n.816G>A (SLC37A4)
ENST00000530407.5:n.1273+5G>A (SLC37A4)
ENST00000532085.1:n.5141+5G>A (SLC37A4)
ENST00000533058.5:c.*137C>T (TRAPPC4) ENSP00000432920.1:n.*137C>T
ENST00000538950.5:c.904+5G>A (SLC37A4) ENSP00000475991.2:n.904+5G>A
ENST00000545985.5:c.1123+5G>A (SLC37A4) ENSP00000475241.2:n.1123+5G>A
NM_001164277.1:c.1123+5G>A , LRG_187t1:c.1123+5G>A (SLC37A4) NP_001157749.1:n.1123+5G>A
NM_001164278.1:c.1189+5G>A (SLC37A4) NP_001157750.1:n.1189+5G>A
NM_001164279.1:c.904+5G>A (SLC37A4) NP_001157751.1:n.904+5G>A
NM_001164280.1:c.1123+5G>A (SLC37A4) NP_001157752.1:n.1123+5G>A
NM_001467.5:c.1123+5G>A (SLC37A4) NP_001458.1:n.1123+5G>A
NM_001164278.2:c.1189+5G>A (SLC37A4) NP_001157750.1:n.1189+5G>A
NM_001164279.2:c.904+5G>A (SLC37A4) NP_001157751.1:n.904+5G>A
NM_001164280.2:c.1123+5G>A (SLC37A4) NP_001157752.1:n.1123+5G>A
NM_001467.6:c.1123+5G>A (SLC37A4) NP_001458.1:n.1123+5G>A
NM_001164277.2:c.1123+5G>A (SLC37A4) MANE Select NP_001157749.1:n.1123+5G>A