Canonical Allele Identifier: CA2616339453

Gene: SLC37A4 TRAPPC4

Linked Data

• gnomAD v4: 11-119024769-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119024769A>G , CM000673.2:g.119024769A>G	GRCh38
NC_000011.9:g.118895479A>G , CM000673.1:g.118895479A>G	GRCh37
NC_000011.8:g.118400689A>G	NCBI36
NG_013331.1:g.11137T>C , LRG_187:g.11137T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1641T>C (SLC37A4)
ENST00000697845.1:n.2630T>C (SLC37A4)
ENST00000697846.1:n.2003T>C (SLC37A4)
ENST00000697847.1:n.1714T>C (SLC37A4)
ENST00000697849.1:n.4107T>C (SLC37A4)
ENST00000697850.1:n.2298T>C (SLC37A4)
ENST00000697851.1:n.3269T>C (SLC37A4)
ENST00000638186.1:n.1735T>C (SLC37A4)
ENST00000638360.1:n.1567T>C (SLC37A4)
ENST00000638925.1:n.1700T>C (SLC37A4)
ENST00000650539.1:n.1903T>C (SLC37A4)
ENST00000330775.9:c.*141T>C (SLC37A4)	ENSP00000476242.2:n.*141T>C
ENST00000357590.9:c.*141T>C (SLC37A4)	ENSP00000476176.2:n.*141T>C
ENST00000525102.5:n.2189T>C (SLC37A4)
ENST00000526275.5:n.2213T>C (SLC37A4)
ENST00000527992.5:n.1659T>C (SLC37A4)
ENST00000532085.1:n.5449T>C (SLC37A4)
ENST00000533058.5:c.582-88A>G (TRAPPC4)	ENSP00000432920.1:n.582-88A>G
ENST00000538950.5:c.*141T>C (SLC37A4)	ENSP00000475991.2:n.*141T>C
ENST00000545985.5:c.*141T>C (SLC37A4)	ENSP00000475241.2:n.*141T>C
NM_001164277.1:c.*141T>C , LRG_187t1:c.*141T>C (SLC37A4)	NP_001157749.1:n.*141T>C
NM_001164278.1:c.*141T>C (SLC37A4)	NP_001157750.1:n.*141T>C
NM_001164279.1:c.*141T>C (SLC37A4)	NP_001157751.1:n.*141T>C
NM_001164280.1:c.*141T>C (SLC37A4)	NP_001157752.1:n.*141T>C
NM_001467.5:c.*141T>C (SLC37A4)	NP_001458.1:n.*141T>C
NM_001164278.2:c.*141T>C (SLC37A4)	NP_001157750.1:n.*141T>C
NM_001164279.2:c.*141T>C (SLC37A4)	NP_001157751.1:n.*141T>C
NM_001164280.2:c.*141T>C (SLC37A4)	NP_001157752.1:n.*141T>C
NM_001467.6:c.*141T>C (SLC37A4)	NP_001458.1:n.*141T>C
NM_001164277.2:c.*141T>C (SLC37A4) MANE Select	NP_001157749.1:n.*141T>C