Canonical Allele Identifier: CA382892656

Gene: SLC37A4 TRAPPC4

Linked Data

• gnomAD v4: 11-119024873-G-T
• MyVariant Identifiers: chr11:g.118895583G>T (hg19) ; chr11:g.119024873G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119024873G>T , CM000673.2:g.119024873G>T	GRCh38
NC_000011.9:g.118895583G>T , CM000673.1:g.118895583G>T	GRCh37
NC_000011.8:g.118400793G>T	NCBI36
NG_013331.1:g.11033C>A , LRG_187:g.11033C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1537C>A (SLC37A4)
ENST00000697845.1:n.2526C>A (SLC37A4)
ENST00000697846.1:n.1899C>A (SLC37A4)
ENST00000697847.1:n.1610C>A (SLC37A4)
ENST00000697849.1:n.4003C>A (SLC37A4)
ENST00000697850.1:n.2194C>A (SLC37A4)
ENST00000697851.1:n.3165C>A (SLC37A4)
ENST00000638186.1:n.1631C>A (SLC37A4)
ENST00000638360.1:n.1463C>A (SLC37A4)
ENST00000638925.1:n.1596C>A (SLC37A4)
ENST00000650539.1:n.1799C>A (SLC37A4)
ENST00000330775.9:c.*37C>A (SLC37A4)	ENSP00000476242.2:n.*37C>A
ENST00000357590.9:c.*37C>A (SLC37A4)	ENSP00000476176.2:n.*37C>A
ENST00000525102.5:n.2085C>A (SLC37A4)
ENST00000526275.5:n.2109C>A (SLC37A4)
ENST00000527992.5:n.1555C>A (SLC37A4)
ENST00000532085.1:n.5345C>A (SLC37A4)
ENST00000533058.5:c.598G>T (TRAPPC4)	ENSP00000432920.1:p.Ala200Ser
ENST00000538950.5:c.*37C>A (SLC37A4)	ENSP00000475991.2:n.*37C>A
ENST00000545985.5:c.*37C>A (SLC37A4)	ENSP00000475241.2:n.*37C>A
NM_001164277.1:c.*37C>A , LRG_187t1:c.*37C>A (SLC37A4)	NP_001157749.1:n.*37C>A
NM_001164278.1:c.*37C>A (SLC37A4)	NP_001157750.1:n.*37C>A
NM_001164279.1:c.*37C>A (SLC37A4)	NP_001157751.1:n.*37C>A
NM_001164280.1:c.*37C>A (SLC37A4)	NP_001157752.1:n.*37C>A
NM_001467.5:c.*37C>A (SLC37A4)	NP_001458.1:n.*37C>A
NM_001164278.2:c.*37C>A (SLC37A4)	NP_001157750.1:n.*37C>A
NM_001164279.2:c.*37C>A (SLC37A4)	NP_001157751.1:n.*37C>A
NM_001164280.2:c.*37C>A (SLC37A4)	NP_001157752.1:n.*37C>A
NM_001467.6:c.*37C>A (SLC37A4)	NP_001458.1:n.*37C>A
NM_001164277.2:c.*37C>A (SLC37A4) MANE Select	NP_001157749.1:n.*37C>A