Canonical Allele Identifier: CA2840523320
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025148C>T , CM000673.2:g.119025148C>T GRCh38
NC_000011.9:g.118895858C>T , CM000673.1:g.118895858C>T GRCh37
NC_000011.8:g.118401068C>T NCBI36
NG_013331.1:g.10758G>A , LRG_187:g.10758G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1333+43G>A (SLC37A4)
ENST00000697845.1:n.2322+43G>A (SLC37A4)
ENST00000697846.1:n.1695+43G>A (SLC37A4)
ENST00000697847.1:n.1406+43G>A (SLC37A4)
ENST00000697849.1:n.3799+43G>A (SLC37A4)
ENST00000697850.1:n.1990+43G>A (SLC37A4)
ENST00000697851.1:n.2961+43G>A (SLC37A4)
ENST00000638186.1:n.1427+43G>A (SLC37A4)
ENST00000638360.1:n.1259+43G>A (SLC37A4)
ENST00000638925.1:n.1392+43G>A (SLC37A4)
ENST00000650539.1:n.1595+43G>A (SLC37A4)
ENST00000330775.9:c.1123+43G>A (SLC37A4) ENSP00000476242.2:n.1123+43G>A
ENST00000357590.9:c.1189+43G>A (SLC37A4) ENSP00000476176.2:n.1189+43G>A
ENST00000524428.5:n.1359+43G>A (SLC37A4)
ENST00000525039.5:n.1613+43G>A (SLC37A4)
ENST00000525102.5:n.1881+43G>A (SLC37A4)
ENST00000525372.5:n.1221+43G>A (SLC37A4)
ENST00000526275.5:n.1905+43G>A (SLC37A4)
ENST00000527992.5:n.1351+43G>A (SLC37A4)
ENST00000530407.5:n.1273+43G>A (SLC37A4)
ENST00000532085.1:n.5141+43G>A (SLC37A4)
ENST00000533058.5:c.*99C>T (TRAPPC4) ENSP00000432920.1:n.*99C>T
ENST00000538950.5:c.904+43G>A (SLC37A4) ENSP00000475991.2:n.904+43G>A
ENST00000545985.5:c.1123+43G>A (SLC37A4) ENSP00000475241.2:n.1123+43G>A
NM_001164277.1:c.1123+43G>A , LRG_187t1:c.1123+43G>A (SLC37A4) NP_001157749.1:n.1123+43G>A
NM_001164278.1:c.1189+43G>A (SLC37A4) NP_001157750.1:n.1189+43G>A
NM_001164279.1:c.904+43G>A (SLC37A4) NP_001157751.1:n.904+43G>A
NM_001164280.1:c.1123+43G>A (SLC37A4) NP_001157752.1:n.1123+43G>A
NM_001467.5:c.1123+43G>A (SLC37A4) NP_001458.1:n.1123+43G>A
NM_001164278.2:c.1189+43G>A (SLC37A4) NP_001157750.1:n.1189+43G>A
NM_001164279.2:c.904+43G>A (SLC37A4) NP_001157751.1:n.904+43G>A
NM_001164280.2:c.1123+43G>A (SLC37A4) NP_001157752.1:n.1123+43G>A
NM_001467.6:c.1123+43G>A (SLC37A4) NP_001458.1:n.1123+43G>A
NM_001164277.2:c.1123+43G>A (SLC37A4) MANE Select NP_001157749.1:n.1123+43G>A