Canonical Allele Identifier: CA382895942

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118895981A>T (hg19) ; chr11:g.119025271A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025271A>T , CM000673.2:g.119025271A>T	GRCh38
NC_000011.9:g.118895981A>T , CM000673.1:g.118895981A>T	GRCh37
NC_000011.8:g.118401191A>T	NCBI36
NG_013331.1:g.10635T>A , LRG_187:g.10635T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1253T>A (SLC37A4)
ENST00000697845.1:n.2242T>A (SLC37A4)
ENST00000697846.1:n.1615T>A (SLC37A4)
ENST00000697847.1:n.1326T>A (SLC37A4)
ENST00000697849.1:n.3719T>A (SLC37A4)
ENST00000697850.1:n.1910T>A (SLC37A4)
ENST00000697851.1:n.2881T>A (SLC37A4)
ENST00000638186.1:n.1347T>A (SLC37A4)
ENST00000638360.1:n.1179T>A (SLC37A4)
ENST00000638925.1:n.1312T>A (SLC37A4)
ENST00000650539.1:n.1515T>A (SLC37A4)
ENST00000330775.9:c.1043T>A (SLC37A4)	ENSP00000476242.2:p.Leu348Gln
ENST00000357590.9:c.1109T>A (SLC37A4)	ENSP00000476176.2:p.Leu370Gln
ENST00000524428.5:n.1279T>A (SLC37A4)
ENST00000525039.5:n.1533T>A (SLC37A4)
ENST00000525102.5:n.1801T>A (SLC37A4)
ENST00000525372.5:n.1141T>A (SLC37A4)
ENST00000526275.5:n.1825T>A (SLC37A4)
ENST00000527992.5:n.1271T>A (SLC37A4)
ENST00000529510.5:n.731T>A (SLC37A4)
ENST00000530407.5:n.1193T>A (SLC37A4)
ENST00000532085.1:n.5061T>A (SLC37A4)
ENST00000533058.5:c.*222A>T (TRAPPC4)	ENSP00000432920.1:n.*222A>T
ENST00000538950.5:c.824T>A (SLC37A4)	ENSP00000475991.2:p.Leu275Gln
ENST00000545985.5:c.1043T>A (SLC37A4)	ENSP00000475241.2:p.Leu348Gln
NM_001164277.1:c.1043T>A , LRG_187t1:c.1043T>A (SLC37A4)	NP_001157749.1:p.Leu348Gln
NM_001164278.1:c.1109T>A (SLC37A4)	NP_001157750.1:p.Leu370Gln
NM_001164279.1:c.824T>A (SLC37A4)	NP_001157751.1:p.Leu275Gln
NM_001164280.1:c.1043T>A (SLC37A4)	NP_001157752.1:p.Leu348Gln
NM_001467.5:c.1043T>A (SLC37A4)	NP_001458.1:p.Leu348Gln
NM_001164278.2:c.1109T>A (SLC37A4)	NP_001157750.1:p.Leu370Gln
NM_001164279.2:c.824T>A (SLC37A4)	NP_001157751.1:p.Leu275Gln
NM_001164280.2:c.1043T>A (SLC37A4)	NP_001157752.1:p.Leu348Gln
NM_001467.6:c.1043T>A (SLC37A4)	NP_001458.1:p.Leu348Gln
NM_001164277.2:c.1043T>A (SLC37A4) MANE Select	NP_001157749.1:p.Leu348Gln