Canonical Allele Identifier: CA2616339569
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Linked Data

dbSNP Id: rs1555190417

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025134G>T , CM000673.2:g.119025134G>T GRCh38
NC_000011.9:g.118895844G>T , CM000673.1:g.118895844G>T GRCh37
NC_000011.8:g.118401054G>T NCBI36
NG_013331.1:g.10772C>A , LRG_187:g.10772C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.1334-58C>A (SLC37A4)
ENST00000697845.1:n.2323-58C>A (SLC37A4)
ENST00000697846.1:n.1696-58C>A (SLC37A4)
ENST00000697847.1:n.1407-58C>A (SLC37A4)
ENST00000697849.1:n.3800-58C>A (SLC37A4)
ENST00000697850.1:n.1991-58C>A (SLC37A4)
ENST00000697851.1:n.2962-58C>A (SLC37A4)
ENST00000638186.1:n.1428-58C>A (SLC37A4)
ENST00000638360.1:n.1260-58C>A (SLC37A4)
ENST00000638925.1:n.1393-58C>A (SLC37A4)
ENST00000650539.1:n.1596-58C>A (SLC37A4)
ENST00000330775.9:c.1124-58C>A (SLC37A4) ENSP00000476242.2:n.1124-58C>A
ENST00000357590.9:c.1190-58C>A (SLC37A4) ENSP00000476176.2:n.1190-58C>A
ENST00000524428.5:n.1360-58C>A (SLC37A4)
ENST00000525039.5:n.1614-58C>A (SLC37A4)
ENST00000525102.5:n.1882-58C>A (SLC37A4)
ENST00000525372.5:n.1222-58C>A (SLC37A4)
ENST00000526275.5:n.1906-58C>A (SLC37A4)
ENST00000527992.5:n.1352-58C>A (SLC37A4)
ENST00000530407.5:n.1274-58C>A (SLC37A4)
ENST00000532085.1:n.5142-58C>A (SLC37A4)
ENST00000533058.5:c.*85G>T (TRAPPC4) ENSP00000432920.1:n.*85G>T
ENST00000538950.5:c.905-58C>A (SLC37A4) ENSP00000475991.2:n.905-58C>A
ENST00000545985.5:c.1124-58C>A (SLC37A4) ENSP00000475241.2:n.1124-58C>A
NM_001164277.1:c.1124-58C>A , LRG_187t1:c.1124-58C>A (SLC37A4) NP_001157749.1:n.1124-58C>A
NM_001164278.1:c.1190-58C>A (SLC37A4) NP_001157750.1:n.1190-58C>A
NM_001164279.1:c.905-58C>A (SLC37A4) NP_001157751.1:n.905-58C>A
NM_001164280.1:c.1124-58C>A (SLC37A4) NP_001157752.1:n.1124-58C>A
NM_001467.5:c.1124-58C>A (SLC37A4) NP_001458.1:n.1124-58C>A
NM_001164278.2:c.1190-58C>A (SLC37A4) NP_001157750.1:n.1190-58C>A
NM_001164279.2:c.905-58C>A (SLC37A4) NP_001157751.1:n.905-58C>A
NM_001164280.2:c.1124-58C>A (SLC37A4) NP_001157752.1:n.1124-58C>A
NM_001467.6:c.1124-58C>A (SLC37A4) NP_001458.1:n.1124-58C>A
NM_001164277.2:c.1124-58C>A (SLC37A4) MANE Select NP_001157749.1:n.1124-58C>A