Canonical Allele Identifier: CA2616339513

Gene: SLC37A4 TRAPPC4

Linked Data

• gnomAD v4: 11-119024823-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119024823C>T , CM000673.2:g.119024823C>T	GRCh38
NC_000011.9:g.118895533C>T , CM000673.1:g.118895533C>T	GRCh37
NC_000011.8:g.118400743C>T	NCBI36
NG_013331.1:g.11083G>A , LRG_187:g.11083G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1587G>A (SLC37A4)
ENST00000697845.1:n.2576G>A (SLC37A4)
ENST00000697846.1:n.1949G>A (SLC37A4)
ENST00000697847.1:n.1660G>A (SLC37A4)
ENST00000697849.1:n.4053G>A (SLC37A4)
ENST00000697850.1:n.2244G>A (SLC37A4)
ENST00000697851.1:n.3215G>A (SLC37A4)
ENST00000638186.1:n.1681G>A (SLC37A4)
ENST00000638360.1:n.1513G>A (SLC37A4)
ENST00000638925.1:n.1646G>A (SLC37A4)
ENST00000650539.1:n.1849G>A (SLC37A4)
ENST00000330775.9:c.*87G>A (SLC37A4)	ENSP00000476242.2:n.*87G>A
ENST00000357590.9:c.*87G>A (SLC37A4)	ENSP00000476176.2:n.*87G>A
ENST00000525102.5:n.2135G>A (SLC37A4)
ENST00000526275.5:n.2159G>A (SLC37A4)
ENST00000527992.5:n.1605G>A (SLC37A4)
ENST00000532085.1:n.5395G>A (SLC37A4)
ENST00000533058.5:c.582-34C>T (TRAPPC4)	ENSP00000432920.1:n.582-34C>T
ENST00000538950.5:c.*87G>A (SLC37A4)	ENSP00000475991.2:n.*87G>A
ENST00000545985.5:c.*87G>A (SLC37A4)	ENSP00000475241.2:n.*87G>A
NM_001164277.1:c.*87G>A , LRG_187t1:c.*87G>A (SLC37A4)	NP_001157749.1:n.*87G>A
NM_001164278.1:c.*87G>A (SLC37A4)	NP_001157750.1:n.*87G>A
NM_001164279.1:c.*87G>A (SLC37A4)	NP_001157751.1:n.*87G>A
NM_001164280.1:c.*87G>A (SLC37A4)	NP_001157752.1:n.*87G>A
NM_001467.5:c.*87G>A (SLC37A4)	NP_001458.1:n.*87G>A
NM_001164278.2:c.*87G>A (SLC37A4)	NP_001157750.1:n.*87G>A
NM_001164279.2:c.*87G>A (SLC37A4)	NP_001157751.1:n.*87G>A
NM_001164280.2:c.*87G>A (SLC37A4)	NP_001157752.1:n.*87G>A
NM_001467.6:c.*87G>A (SLC37A4)	NP_001458.1:n.*87G>A
NM_001164277.2:c.*87G>A (SLC37A4) MANE Select	NP_001157749.1:n.*87G>A