Canonical Allele Identifier: CA6311559
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Linked Data

dbSNP Id: rs782504057

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119024860G>A , CM000673.2:g.119024860G>A GRCh38
NC_000011.9:g.118895570G>A , CM000673.1:g.118895570G>A GRCh37
NC_000011.8:g.118400780G>A NCBI36
NG_013331.1:g.11046C>T , LRG_187:g.11046C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1550C>T (SLC37A4)
ENST00000697845.1:n.2539C>T (SLC37A4)
ENST00000697846.1:n.1912C>T (SLC37A4)
ENST00000697847.1:n.1623C>T (SLC37A4)
ENST00000697849.1:n.4016C>T (SLC37A4)
ENST00000697850.1:n.2207C>T (SLC37A4)
ENST00000697851.1:n.3178C>T (SLC37A4)
ENST00000638186.1:n.1644C>T (SLC37A4)
ENST00000638360.1:n.1476C>T (SLC37A4)
ENST00000638925.1:n.1609C>T (SLC37A4)
ENST00000650539.1:n.1812C>T (SLC37A4)
ENST00000330775.9:c.*50C>T (SLC37A4) ENSP00000476242.2:n.*50C>T
ENST00000357590.9:c.*50C>T (SLC37A4) ENSP00000476176.2:n.*50C>T
ENST00000525102.5:n.2098C>T (SLC37A4)
ENST00000526275.5:n.2122C>T (SLC37A4)
ENST00000527992.5:n.1568C>T (SLC37A4)
ENST00000532085.1:n.5358C>T (SLC37A4)
ENST00000533058.5:c.585G>A (TRAPPC4) ENSP00000432920.1:p.Ala195=
ENST00000538950.5:c.*50C>T (SLC37A4) ENSP00000475991.2:n.*50C>T
ENST00000545985.5:c.*50C>T (SLC37A4) ENSP00000475241.2:n.*50C>T
NM_001164277.1:c.*50C>T , LRG_187t1:c.*50C>T (SLC37A4) NP_001157749.1:n.*50C>T
NM_001164278.1:c.*50C>T (SLC37A4) NP_001157750.1:n.*50C>T
NM_001164279.1:c.*50C>T (SLC37A4) NP_001157751.1:n.*50C>T
NM_001164280.1:c.*50C>T (SLC37A4) NP_001157752.1:n.*50C>T
NM_001467.5:c.*50C>T (SLC37A4) NP_001458.1:n.*50C>T
NM_001164278.2:c.*50C>T (SLC37A4) NP_001157750.1:n.*50C>T
NM_001164279.2:c.*50C>T (SLC37A4) NP_001157751.1:n.*50C>T
NM_001164280.2:c.*50C>T (SLC37A4) NP_001157752.1:n.*50C>T
NM_001467.6:c.*50C>T (SLC37A4) NP_001458.1:n.*50C>T
NM_001164277.2:c.*50C>T (SLC37A4) MANE Select NP_001157749.1:n.*50C>T