Canonical Allele Identifier: CA382905808

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028342C>T , CM000673.2:g.119028342C>T	GRCh38
NC_000011.9:g.118899052C>T , CM000673.1:g.118899052C>T	GRCh37
NC_000011.8:g.118404262C>T	NCBI36
NG_013331.1:g.7565G>A , LRG_187:g.7565G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001164277.2:c.233G>A MANE Select	NP_001157749.1:p.Trp78Ter
NM_001164277.1:c.233G>A , LRG_187t1:c.233G>A	NP_001157749.1:p.Trp78Ter
NM_001164278.1:c.233G>A	NP_001157750.1:p.Trp78Ter
NM_001164278.2:c.233G>A	NP_001157750.1:p.Trp78Ter
NM_001164279.1:c.14G>A	NP_001157751.1:p.Trp5Ter
NM_001164279.2:c.14G>A	NP_001157751.1:p.Trp5Ter
NM_001164280.1:c.233G>A	NP_001157752.1:p.Trp78Ter
NM_001164280.2:c.233G>A	NP_001157752.1:p.Trp78Ter
NM_001467.5:c.233G>A	NP_001458.1:p.Trp78Ter
NM_001467.6:c.233G>A	NP_001458.1:p.Trp78Ter
ENST00000330775.9:c.233G>A	ENSP00000476242.2:p.Trp78Ter
ENST00000357590.9:c.233G>A	ENSP00000476176.2:p.Trp78Ter
ENST00000524428.5:n.233G>A
ENST00000525039.5:n.656G>A
ENST00000525102.5:n.990G>A
ENST00000525372.5:n.233G>A
ENST00000525787.1:n.528G>A
ENST00000526275.5:n.693G>A
ENST00000526626.6:n.344-470G>A
ENST00000527992.5:n.460G>A
ENST00000529510.5:n.251G>A
ENST00000529510.6:n.462G>A
ENST00000530407.5:n.382G>A
ENST00000532085.1:n.2522G>A
ENST00000532888.6:n.528G>A
ENST00000534384.1:n.453G>A
ENST00000538950.5:c.14G>A	ENSP00000475991.2:p.Trp5Ter
ENST00000545985.5:c.233G>A	ENSP00000475241.2:p.Trp78Ter
ENST00000638186.1:n.536G>A
ENST00000638360.1:n.470G>A
ENST00000638925.1:n.469G>A
ENST00000650539.1:n.638G>A
ENST00000697845.1:n.386G>A
ENST00000697846.1:n.462G>A
ENST00000697847.1:n.462G>A
ENST00000697848.1:n.462G>A
ENST00000697849.1:n.1501G>A
ENST00000697850.1:n.462G>A
ENST00000697851.1:n.1501G>A