Canonical Allele Identifier: CA382892841

Gene: SLC37A4 TRAPPC4

Linked Data

• dbSNP Id: rs1943500913
• gnomAD v4: 11-119024886-G-T
• MyVariant Identifiers: chr11:g.118895596G>T (hg19) ; chr11:g.119024886G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119024886G>T , CM000673.2:g.119024886G>T	GRCh38
NC_000011.9:g.118895596G>T , CM000673.1:g.118895596G>T	GRCh37
NC_000011.8:g.118400806G>T	NCBI36
NG_013331.1:g.11020C>A , LRG_187:g.11020C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1524C>A (SLC37A4)
ENST00000697845.1:n.2513C>A (SLC37A4)
ENST00000697846.1:n.1886C>A (SLC37A4)
ENST00000697847.1:n.1597C>A (SLC37A4)
ENST00000697849.1:n.3990C>A (SLC37A4)
ENST00000697850.1:n.2181C>A (SLC37A4)
ENST00000697851.1:n.3152C>A (SLC37A4)
ENST00000638186.1:n.1618C>A (SLC37A4)
ENST00000638360.1:n.1450C>A (SLC37A4)
ENST00000638925.1:n.1583C>A (SLC37A4)
ENST00000650539.1:n.1786C>A (SLC37A4)
ENST00000330775.9:c.*24C>A (SLC37A4)	ENSP00000476242.2:n.*24C>A
ENST00000357590.9:c.*24C>A (SLC37A4)	ENSP00000476176.2:n.*24C>A
ENST00000525102.5:n.2072C>A (SLC37A4)
ENST00000526275.5:n.2096C>A (SLC37A4)
ENST00000527992.5:n.1542C>A (SLC37A4)
ENST00000530407.5:n.1464C>A (SLC37A4)
ENST00000532085.1:n.5332C>A (SLC37A4)
ENST00000533058.5:c.611G>T (TRAPPC4)	ENSP00000432920.1:p.Trp204Leu
ENST00000538950.5:c.*24C>A (SLC37A4)	ENSP00000475991.2:n.*24C>A
ENST00000545985.5:c.*24C>A (SLC37A4)	ENSP00000475241.2:n.*24C>A
NM_001164277.1:c.*24C>A , LRG_187t1:c.*24C>A (SLC37A4)	NP_001157749.1:n.*24C>A
NM_001164278.1:c.*24C>A (SLC37A4)	NP_001157750.1:n.*24C>A
NM_001164279.1:c.*24C>A (SLC37A4)	NP_001157751.1:n.*24C>A
NM_001164280.1:c.*24C>A (SLC37A4)	NP_001157752.1:n.*24C>A
NM_001467.5:c.*24C>A (SLC37A4)	NP_001458.1:n.*24C>A
NM_001164278.2:c.*24C>A (SLC37A4)	NP_001157750.1:n.*24C>A
NM_001164279.2:c.*24C>A (SLC37A4)	NP_001157751.1:n.*24C>A
NM_001164280.2:c.*24C>A (SLC37A4)	NP_001157752.1:n.*24C>A
NM_001467.6:c.*24C>A (SLC37A4)	NP_001458.1:n.*24C>A
NM_001164277.2:c.*24C>A (SLC37A4) MANE Select	NP_001157749.1:n.*24C>A