Canonical Allele Identifier: CA942779313

Gene: SLC37A4 TRAPPC4

Linked Data

• dbSNP Id: rs1943494490
• gnomAD v3: 11-119024700-C-T
• gnomAD v4: 11-119024700-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119024700C>T , CM000673.2:g.119024700C>T	GRCh38
NC_000011.9:g.118895410C>T , CM000673.1:g.118895410C>T	GRCh37
NC_000011.8:g.118400620C>T	NCBI36
NG_013331.1:g.11206G>A , LRG_187:g.11206G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1710G>A (SLC37A4)
ENST00000697845.1:n.2699G>A (SLC37A4)
ENST00000697846.1:n.2072G>A (SLC37A4)
ENST00000697847.1:n.1783G>A (SLC37A4)
ENST00000697849.1:n.4176G>A (SLC37A4)
ENST00000697850.1:n.2367G>A (SLC37A4)
ENST00000697851.1:n.3338G>A (SLC37A4)
ENST00000638186.1:n.1804G>A (SLC37A4)
ENST00000638360.1:n.1636G>A (SLC37A4)
ENST00000638925.1:n.1769G>A (SLC37A4)
ENST00000650539.1:n.1972G>A (SLC37A4)
ENST00000330775.9:c.*210G>A (SLC37A4)	ENSP00000476242.2:n.*210G>A
ENST00000357590.9:c.*210G>A (SLC37A4)	ENSP00000476176.2:n.*210G>A
ENST00000525102.5:n.2258G>A (SLC37A4)
ENST00000526275.5:n.2282G>A (SLC37A4)
ENST00000527992.5:n.1728G>A (SLC37A4)
ENST00000532085.1:n.5518G>A (SLC37A4)
ENST00000533058.5:c.582-157C>T (TRAPPC4)	ENSP00000432920.1:n.582-157C>T
ENST00000538950.5:c.*210G>A (SLC37A4)	ENSP00000475991.2:n.*210G>A
ENST00000545985.5:c.*210G>A (SLC37A4)	ENSP00000475241.2:n.*210G>A
NM_001164277.1:c.*210G>A , LRG_187t1:c.*210G>A (SLC37A4)	NP_001157749.1:n.*210G>A
NM_001164278.1:c.*210G>A (SLC37A4)	NP_001157750.1:n.*210G>A
NM_001164279.1:c.*210G>A (SLC37A4)	NP_001157751.1:n.*210G>A
NM_001164280.1:c.*210G>A (SLC37A4)	NP_001157752.1:n.*210G>A
NM_001467.5:c.*210G>A (SLC37A4)	NP_001458.1:n.*210G>A
NM_001164278.2:c.*210G>A (SLC37A4)	NP_001157750.1:n.*210G>A
NM_001164279.2:c.*210G>A (SLC37A4)	NP_001157751.1:n.*210G>A
NM_001164280.2:c.*210G>A (SLC37A4)	NP_001157752.1:n.*210G>A
NM_001467.6:c.*210G>A (SLC37A4)	NP_001458.1:n.*210G>A
NM_001164277.2:c.*210G>A (SLC37A4) MANE Select	NP_001157749.1:n.*210G>A