Canonical Allele Identifier: CA382901526

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118897767G>T (hg19) ; chr11:g.119027057G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027057G>T , CM000673.2:g.119027057G>T	GRCh38
NC_000011.9:g.118897767G>T , CM000673.1:g.118897767G>T	GRCh37
NC_000011.8:g.118402977G>T	NCBI36
NG_013331.1:g.8849C>A , LRG_187:g.8849C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.894C>A
ENST00000697845.1:n.818C>A
ENST00000697846.1:n.894C>A
ENST00000697847.1:n.894C>A
ENST00000697848.1:n.894C>A
ENST00000697849.1:n.1933C>A
ENST00000697850.1:n.894C>A
ENST00000697851.1:n.2254C>A
ENST00000638186.1:n.968C>A
ENST00000638360.1:n.800C>A
ENST00000638925.1:n.901C>A
ENST00000650539.1:n.1070C>A
ENST00000330775.9:c.664C>A	ENSP00000476242.2:p.Leu222Met
ENST00000357590.9:c.664C>A	ENSP00000476176.2:p.Leu222Met
ENST00000524428.5:n.986C>A
ENST00000525039.5:n.1088C>A
ENST00000525102.5:n.1422C>A
ENST00000525372.5:n.665C>A
ENST00000526275.5:n.1446C>A
ENST00000526626.6:n.627C>A
ENST00000527992.5:n.892C>A
ENST00000529510.5:n.438C>A
ENST00000530407.5:n.814C>A
ENST00000532085.1:n.3275C>A
ENST00000532888.6:n.960C>A
ENST00000538950.5:c.445C>A	ENSP00000475991.2:p.Leu149Met
ENST00000545985.5:c.664C>A	ENSP00000475241.2:p.Leu222Met
NM_001164277.1:c.664C>A , LRG_187t1:c.664C>A	NP_001157749.1:p.Leu222Met
NM_001164278.1:c.664C>A	NP_001157750.1:p.Leu222Met
NM_001164279.1:c.445C>A	NP_001157751.1:p.Leu149Met
NM_001164280.1:c.664C>A	NP_001157752.1:p.Leu222Met
NM_001467.5:c.664C>A	NP_001458.1:p.Leu222Met
NM_001164278.2:c.664C>A	NP_001157750.1:p.Leu222Met
NM_001164279.2:c.445C>A	NP_001157751.1:p.Leu149Met
NM_001164280.2:c.664C>A	NP_001157752.1:p.Leu222Met
NM_001467.6:c.664C>A	NP_001458.1:p.Leu222Met
NM_001164277.2:c.664C>A MANE Select	NP_001157749.1:p.Leu222Met