Canonical Allele Identifier: CA2003748347
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Linked Data

dbSNP Id: rs1943516379

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025118C>A , CM000673.2:g.119025118C>A GRCh38
NC_000011.9:g.118895828C>A , CM000673.1:g.118895828C>A GRCh37
NC_000011.8:g.118401038C>A NCBI36
NG_013331.1:g.10788G>T , LRG_187:g.10788G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.1334-42G>T (SLC37A4)
ENST00000697845.1:n.2323-42G>T (SLC37A4)
ENST00000697846.1:n.1696-42G>T (SLC37A4)
ENST00000697847.1:n.1407-42G>T (SLC37A4)
ENST00000697849.1:n.3800-42G>T (SLC37A4)
ENST00000697850.1:n.1991-42G>T (SLC37A4)
ENST00000697851.1:n.2962-42G>T (SLC37A4)
ENST00000638186.1:n.1428-42G>T (SLC37A4)
ENST00000638360.1:n.1260-42G>T (SLC37A4)
ENST00000638925.1:n.1393-42G>T (SLC37A4)
ENST00000650539.1:n.1596-42G>T (SLC37A4)
ENST00000330775.9:c.1124-42G>T (SLC37A4) ENSP00000476242.2:n.1124-42G>T
ENST00000357590.9:c.1190-42G>T (SLC37A4) ENSP00000476176.2:n.1190-42G>T
ENST00000524428.5:n.1360-42G>T (SLC37A4)
ENST00000525039.5:n.1614-42G>T (SLC37A4)
ENST00000525102.5:n.1882-42G>T (SLC37A4)
ENST00000525372.5:n.1222-42G>T (SLC37A4)
ENST00000526275.5:n.1906-42G>T (SLC37A4)
ENST00000527992.5:n.1352-42G>T (SLC37A4)
ENST00000530407.5:n.1274-42G>T (SLC37A4)
ENST00000532085.1:n.5142-42G>T (SLC37A4)
ENST00000533058.5:c.*69C>A (TRAPPC4) ENSP00000432920.1:n.*69C>A
ENST00000538950.5:c.905-42G>T (SLC37A4) ENSP00000475991.2:n.905-42G>T
ENST00000545985.5:c.1124-42G>T (SLC37A4) ENSP00000475241.2:n.1124-42G>T
NM_001164277.1:c.1124-42G>T , LRG_187t1:c.1124-42G>T (SLC37A4) NP_001157749.1:n.1124-42G>T
NM_001164278.1:c.1190-42G>T (SLC37A4) NP_001157750.1:n.1190-42G>T
NM_001164279.1:c.905-42G>T (SLC37A4) NP_001157751.1:n.905-42G>T
NM_001164280.1:c.1124-42G>T (SLC37A4) NP_001157752.1:n.1124-42G>T
NM_001467.5:c.1124-42G>T (SLC37A4) NP_001458.1:n.1124-42G>T
NM_001164278.2:c.1190-42G>T (SLC37A4) NP_001157750.1:n.1190-42G>T
NM_001164279.2:c.905-42G>T (SLC37A4) NP_001157751.1:n.905-42G>T
NM_001164280.2:c.1124-42G>T (SLC37A4) NP_001157752.1:n.1124-42G>T
NM_001467.6:c.1124-42G>T (SLC37A4) NP_001458.1:n.1124-42G>T
NM_001164277.2:c.1124-42G>T (SLC37A4) MANE Select NP_001157749.1:n.1124-42G>T