Canonical Allele Identifier: CA382904424

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118898905T>C (hg19) ; chr11:g.119028195T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028195T>C , CM000673.2:g.119028195T>C	GRCh38
NC_000011.9:g.118898905T>C , CM000673.1:g.118898905T>C	GRCh37
NC_000011.8:g.118404115T>C	NCBI36
NG_013331.1:g.7712A>G , LRG_187:g.7712A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.609A>G
ENST00000697845.1:n.533A>G
ENST00000697846.1:n.609A>G
ENST00000697847.1:n.609A>G
ENST00000697848.1:n.609A>G
ENST00000697849.1:n.1648A>G
ENST00000697850.1:n.609A>G
ENST00000697851.1:n.1648A>G
ENST00000638186.1:n.683A>G
ENST00000638360.1:n.617A>G
ENST00000638925.1:n.616A>G
ENST00000650539.1:n.785A>G
ENST00000330775.9:c.380A>G	ENSP00000476242.2:p.Lys127Arg
ENST00000357590.9:c.380A>G	ENSP00000476176.2:p.Lys127Arg
ENST00000524428.5:n.380A>G
ENST00000525039.5:n.803A>G
ENST00000525102.5:n.1137A>G
ENST00000525372.5:n.380A>G
ENST00000525787.1:n.675A>G
ENST00000526275.5:n.840A>G
ENST00000526626.6:n.344-323A>G
ENST00000527992.5:n.607A>G
ENST00000529510.5:n.398A>G
ENST00000530407.5:n.529A>G
ENST00000532085.1:n.2669A>G
ENST00000532888.6:n.675A>G
ENST00000538950.5:c.161A>G	ENSP00000475991.2:p.Lys54Arg
ENST00000545985.5:c.380A>G	ENSP00000475241.2:p.Lys127Arg
NM_001164277.1:c.380A>G , LRG_187t1:c.380A>G	NP_001157749.1:p.Lys127Arg
NM_001164278.1:c.380A>G	NP_001157750.1:p.Lys127Arg
NM_001164279.1:c.161A>G	NP_001157751.1:p.Lys54Arg
NM_001164280.1:c.380A>G	NP_001157752.1:p.Lys127Arg
NM_001467.5:c.380A>G	NP_001458.1:p.Lys127Arg
NM_001164278.2:c.380A>G	NP_001157750.1:p.Lys127Arg
NM_001164279.2:c.161A>G	NP_001157751.1:p.Lys54Arg
NM_001164280.2:c.380A>G	NP_001157752.1:p.Lys127Arg
NM_001467.6:c.380A>G	NP_001458.1:p.Lys127Arg
NM_001164277.2:c.380A>G MANE Select	NP_001157749.1:p.Lys127Arg