Canonical Allele Identifier: CA2003748219
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119024879G= , CM000673.2:g.119024879G= GRCh38
NC_000011.9:g.118895589G= , CM000673.1:g.118895589G= GRCh37
NC_000011.8:g.118400799G= NCBI36
NG_013331.1:g.11027C= , LRG_187:g.11027C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1531C= (SLC37A4)
ENST00000697845.1:n.2520C= (SLC37A4)
ENST00000697846.1:n.1893C= (SLC37A4)
ENST00000697847.1:n.1604C= (SLC37A4)
ENST00000697849.1:n.3997C= (SLC37A4)
ENST00000697850.1:n.2188C= (SLC37A4)
ENST00000697851.1:n.3159C= (SLC37A4)
ENST00000638186.1:n.1625C= (SLC37A4)
ENST00000638360.1:n.1457C= (SLC37A4)
ENST00000638925.1:n.1590C= (SLC37A4)
ENST00000650539.1:n.1793C= (SLC37A4)
ENST00000330775.9:c.*31C= (SLC37A4) ENSP00000476242.2:n.*31C=
ENST00000357590.9:c.*31C= (SLC37A4) ENSP00000476176.2:n.*31C=
ENST00000525102.5:n.2079C= (SLC37A4)
ENST00000526275.5:n.2103C= (SLC37A4)
ENST00000527992.5:n.1549C= (SLC37A4)
ENST00000530407.5:n.1471C= (SLC37A4)
ENST00000532085.1:n.5339C= (SLC37A4)
ENST00000533058.5:c.604G= (TRAPPC4) ENSP00000432920.1:p.Val202=
ENST00000538950.5:c.*31C= (SLC37A4) ENSP00000475991.2:n.*31C=
ENST00000545985.5:c.*31C= (SLC37A4) ENSP00000475241.2:n.*31C=
NM_001164277.1:c.*31C= , LRG_187t1:c.*31C= (SLC37A4) NP_001157749.1:n.*31C=
NM_001164278.1:c.*31C= (SLC37A4) NP_001157750.1:n.*31C=
NM_001164279.1:c.*31C= (SLC37A4) NP_001157751.1:n.*31C=
NM_001164280.1:c.*31C= (SLC37A4) NP_001157752.1:n.*31C=
NM_001467.5:c.*31C= (SLC37A4) NP_001458.1:n.*31C=
NM_001164278.2:c.*31C= (SLC37A4) NP_001157750.1:n.*31C=
NM_001164279.2:c.*31C= (SLC37A4) NP_001157751.1:n.*31C=
NM_001164280.2:c.*31C= (SLC37A4) NP_001157752.1:n.*31C=
NM_001467.6:c.*31C= (SLC37A4) NP_001458.1:n.*31C=
NM_001164277.2:c.*31C= (SLC37A4) MANE Select NP_001157749.1:n.*31C=