Canonical Allele Identifier: CA382904034

Gene: SLC37A4

Linked Data

• dbSNP Id: rs193302896
• MyVariant Identifiers: chr11:g.118898566T>C (hg19) ; chr11:g.119027856T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027856T>C , CM000673.2:g.119027856T>C	GRCh38
NC_000011.9:g.118898566T>C , CM000673.1:g.118898566T>C	GRCh37
NC_000011.8:g.118403776T>C	NCBI36
NG_013331.1:g.8051A>G , LRG_187:g.8051A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.627A>G
ENST00000697845.1:n.551A>G
ENST00000697846.1:n.627A>G
ENST00000697847.1:n.627A>G
ENST00000697848.1:n.627A>G
ENST00000697849.1:n.1666A>G
ENST00000697850.1:n.627A>G
ENST00000697851.1:n.1987A>G
ENST00000638186.1:n.701A>G
ENST00000638360.1:n.619-86A>G
ENST00000638925.1:n.634A>G
ENST00000650539.1:n.803A>G
ENST00000330775.9:c.398A>G	ENSP00000476242.2:p.Gln133Arg
ENST00000357590.9:c.398A>G	ENSP00000476176.2:p.Gln133Arg
ENST00000524428.5:n.719A>G
ENST00000525039.5:n.821A>G
ENST00000525102.5:n.1155A>G
ENST00000525372.5:n.398A>G
ENST00000525787.1:n.1014A>G
ENST00000526275.5:n.1179A>G
ENST00000526626.6:n.360A>G
ENST00000527992.5:n.625A>G
ENST00000529510.5:n.399+338A>G
ENST00000530407.5:n.547A>G
ENST00000532085.1:n.3008A>G
ENST00000532888.6:n.693A>G
ENST00000538950.5:c.179A>G	ENSP00000475991.2:p.Gln60Arg
ENST00000545985.5:c.398A>G	ENSP00000475241.2:p.Gln133Arg
NM_001164277.1:c.398A>G , LRG_187t1:c.398A>G	NP_001157749.1:p.Gln133Arg
NM_001164278.1:c.398A>G	NP_001157750.1:p.Gln133Arg
NM_001164279.1:c.179A>G	NP_001157751.1:p.Gln60Arg
NM_001164280.1:c.398A>G	NP_001157752.1:p.Gln133Arg
NM_001467.5:c.398A>G	NP_001458.1:p.Gln133Arg
NM_001164278.2:c.398A>G	NP_001157750.1:p.Gln133Arg
NM_001164279.2:c.179A>G	NP_001157751.1:p.Gln60Arg
NM_001164280.2:c.398A>G	NP_001157752.1:p.Gln133Arg
NM_001467.6:c.398A>G	NP_001458.1:p.Gln133Arg
NM_001164277.2:c.398A>G MANE Select	NP_001157749.1:p.Gln133Arg