Canonical Allele Identifier: CA382900196

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118897351T>C (hg19) ; chr11:g.119026641T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026641T>C , CM000673.2:g.119026641T>C	GRCh38
NC_000011.9:g.118897351T>C , CM000673.1:g.118897351T>C	GRCh37
NC_000011.8:g.118402561T>C	NCBI36
NG_013331.1:g.9265A>G , LRG_187:g.9265A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1014+296A>G
ENST00000697845.1:n.1234A>G
ENST00000697846.1:n.1014+296A>G
ENST00000697847.1:n.1062A>G
ENST00000697848.1:n.1062A>G
ENST00000697849.1:n.2349A>G
ENST00000697850.1:n.1062A>G
ENST00000697851.1:n.2670A>G
ENST00000638186.1:n.1136A>G
ENST00000638360.1:n.968A>G
ENST00000638925.1:n.1069A>G
ENST00000650539.1:n.1238A>G
ENST00000330775.9:c.832A>G	ENSP00000476242.2:p.Ile278Val
ENST00000357590.9:c.832A>G	ENSP00000476176.2:p.Ile278Val
ENST00000524428.5:n.1106+296A>G
ENST00000525039.5:n.1256A>G
ENST00000525102.5:n.1590A>G
ENST00000525372.5:n.833A>G
ENST00000526275.5:n.1614A>G
ENST00000527992.5:n.1060A>G
ENST00000529510.5:n.558+296A>G
ENST00000530407.5:n.982A>G
ENST00000532085.1:n.3691A>G
ENST00000538950.5:c.613A>G	ENSP00000475991.2:p.Ile205Val
ENST00000545985.5:c.832A>G	ENSP00000475241.2:p.Ile278Val
NM_001164277.1:c.832A>G , LRG_187t1:c.832A>G	NP_001157749.1:p.Ile278Val
NM_001164278.1:c.832A>G	NP_001157750.1:p.Ile278Val
NM_001164279.1:c.613A>G	NP_001157751.1:p.Ile205Val
NM_001164280.1:c.832A>G	NP_001157752.1:p.Ile278Val
NM_001467.5:c.832A>G	NP_001458.1:p.Ile278Val
NM_001164278.2:c.832A>G	NP_001157750.1:p.Ile278Val
NM_001164279.2:c.613A>G	NP_001157751.1:p.Ile205Val
NM_001164280.2:c.832A>G	NP_001157752.1:p.Ile278Val
NM_001467.6:c.832A>G	NP_001458.1:p.Ile278Val
NM_001164277.2:c.832A>G MANE Select	NP_001157749.1:p.Ile278Val