Canonical Allele Identifier: CA912971013

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118897721dup (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027012dup , CM000673.2:g.119027012dup	GRCh38
NC_000011.9:g.118897722dup , CM000673.1:g.118897722dup	GRCh37
NC_000011.8:g.118402932dup	NCBI36
NG_013331.1:g.8896dup , LRG_187:g.8896dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.941dup
ENST00000697845.1:n.865dup
ENST00000697846.1:n.941dup
ENST00000697847.1:n.941dup
ENST00000697848.1:n.941dup
ENST00000697849.1:n.1980dup
ENST00000697850.1:n.941dup
ENST00000697851.1:n.2301dup
ENST00000638186.1:n.1015dup
ENST00000638360.1:n.847dup
ENST00000638925.1:n.948dup
ENST00000650539.1:n.1117dup
ENST00000330775.9:c.711dup	ENSP00000476242.2:p.Gly238TrpfsTer8
ENST00000357590.9:c.711dup	ENSP00000476176.2:p.Gly238TrpfsTer8
ENST00000524428.5:n.1033dup
ENST00000525039.5:n.1135dup
ENST00000525102.5:n.1469dup
ENST00000525372.5:n.712dup
ENST00000526275.5:n.1493dup
ENST00000526626.6:n.674dup
ENST00000527992.5:n.939dup
ENST00000529510.5:n.485dup
ENST00000530407.5:n.861dup
ENST00000532085.1:n.3322dup
ENST00000532888.6:n.1007dup
ENST00000538950.5:c.492dup	ENSP00000475991.2:p.Gly165TrpfsTer8
ENST00000545985.5:c.711dup	ENSP00000475241.2:p.Gly238TrpfsTer8
NM_001164277.1:c.711dup , LRG_187t1:c.711dup	NP_001157749.1:p.Gly238TrpfsTer8
NM_001164278.1:c.711dup	NP_001157750.1:p.Gly238TrpfsTer8
NM_001164279.1:c.492dup	NP_001157751.1:p.Gly165TrpfsTer8
NM_001164280.1:c.711dup	NP_001157752.1:p.Gly238TrpfsTer8
NM_001467.5:c.711dup	NP_001458.1:p.Gly238TrpfsTer8
NM_001164278.2:c.711dup	NP_001157750.1:p.Gly238TrpfsTer8
NM_001164279.2:c.492dup	NP_001157751.1:p.Gly165TrpfsTer8
NM_001164280.2:c.711dup	NP_001157752.1:p.Gly238TrpfsTer8
NM_001467.6:c.711dup	NP_001458.1:p.Gly238TrpfsTer8
NM_001164277.2:c.711dup MANE Select	NP_001157749.1:p.Gly238TrpfsTer8