Canonical Allele Identifier: CA2003748139

Gene: SLC37A4 TRAPPC4

Linked Data

• dbSNP Id: rs1943495435
• gnomAD v4: 11-119024733-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119024733A>G , CM000673.2:g.119024733A>G	GRCh38
NC_000011.9:g.118895443A>G , CM000673.1:g.118895443A>G	GRCh37
NC_000011.8:g.118400653A>G	NCBI36
NG_013331.1:g.11173T>C , LRG_187:g.11173T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1677T>C (SLC37A4)
ENST00000697845.1:n.2666T>C (SLC37A4)
ENST00000697846.1:n.2039T>C (SLC37A4)
ENST00000697847.1:n.1750T>C (SLC37A4)
ENST00000697849.1:n.4143T>C (SLC37A4)
ENST00000697850.1:n.2334T>C (SLC37A4)
ENST00000697851.1:n.3305T>C (SLC37A4)
ENST00000638186.1:n.1771T>C (SLC37A4)
ENST00000638360.1:n.1603T>C (SLC37A4)
ENST00000638925.1:n.1736T>C (SLC37A4)
ENST00000650539.1:n.1939T>C (SLC37A4)
ENST00000330775.9:c.*177T>C (SLC37A4)	ENSP00000476242.2:n.*177T>C
ENST00000357590.9:c.*177T>C (SLC37A4)	ENSP00000476176.2:n.*177T>C
ENST00000525102.5:n.2225T>C (SLC37A4)
ENST00000526275.5:n.2249T>C (SLC37A4)
ENST00000527992.5:n.1695T>C (SLC37A4)
ENST00000532085.1:n.5485T>C (SLC37A4)
ENST00000533058.5:c.582-124A>G (TRAPPC4)	ENSP00000432920.1:n.582-124A>G
ENST00000538950.5:c.*177T>C (SLC37A4)	ENSP00000475991.2:n.*177T>C
ENST00000545985.5:c.*177T>C (SLC37A4)	ENSP00000475241.2:n.*177T>C
NM_001164277.1:c.*177T>C , LRG_187t1:c.*177T>C (SLC37A4)	NP_001157749.1:n.*177T>C
NM_001164278.1:c.*177T>C (SLC37A4)	NP_001157750.1:n.*177T>C
NM_001164279.1:c.*177T>C (SLC37A4)	NP_001157751.1:n.*177T>C
NM_001164280.1:c.*177T>C (SLC37A4)	NP_001157752.1:n.*177T>C
NM_001467.5:c.*177T>C (SLC37A4)	NP_001458.1:n.*177T>C
NM_001164278.2:c.*177T>C (SLC37A4)	NP_001157750.1:n.*177T>C
NM_001164279.2:c.*177T>C (SLC37A4)	NP_001157751.1:n.*177T>C
NM_001164280.2:c.*177T>C (SLC37A4)	NP_001157752.1:n.*177T>C
NM_001467.6:c.*177T>C (SLC37A4)	NP_001458.1:n.*177T>C
NM_001164277.2:c.*177T>C (SLC37A4) MANE Select	NP_001157749.1:n.*177T>C