Canonical Allele Identifier: CA382901487

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118897757T>C (hg19) ; chr11:g.119027047T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027047T>C , CM000673.2:g.119027047T>C	GRCh38
NC_000011.9:g.118897757T>C , CM000673.1:g.118897757T>C	GRCh37
NC_000011.8:g.118402967T>C	NCBI36
NG_013331.1:g.8859A>G , LRG_187:g.8859A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.904A>G
ENST00000697845.1:n.828A>G
ENST00000697846.1:n.904A>G
ENST00000697847.1:n.904A>G
ENST00000697848.1:n.904A>G
ENST00000697849.1:n.1943A>G
ENST00000697850.1:n.904A>G
ENST00000697851.1:n.2264A>G
ENST00000638186.1:n.978A>G
ENST00000638360.1:n.810A>G
ENST00000638925.1:n.911A>G
ENST00000650539.1:n.1080A>G
ENST00000330775.9:c.674A>G	ENSP00000476242.2:p.Tyr225Cys
ENST00000357590.9:c.674A>G	ENSP00000476176.2:p.Tyr225Cys
ENST00000524428.5:n.996A>G
ENST00000525039.5:n.1098A>G
ENST00000525102.5:n.1432A>G
ENST00000525372.5:n.675A>G
ENST00000526275.5:n.1456A>G
ENST00000526626.6:n.637A>G
ENST00000527992.5:n.902A>G
ENST00000529510.5:n.448A>G
ENST00000530407.5:n.824A>G
ENST00000532085.1:n.3285A>G
ENST00000532888.6:n.970A>G
ENST00000538950.5:c.455A>G	ENSP00000475991.2:p.Tyr152Cys
ENST00000545985.5:c.674A>G	ENSP00000475241.2:p.Tyr225Cys
NM_001164277.1:c.674A>G , LRG_187t1:c.674A>G	NP_001157749.1:p.Tyr225Cys
NM_001164278.1:c.674A>G	NP_001157750.1:p.Tyr225Cys
NM_001164279.1:c.455A>G	NP_001157751.1:p.Tyr152Cys
NM_001164280.1:c.674A>G	NP_001157752.1:p.Tyr225Cys
NM_001467.5:c.674A>G	NP_001458.1:p.Tyr225Cys
NM_001164278.2:c.674A>G	NP_001157750.1:p.Tyr225Cys
NM_001164279.2:c.455A>G	NP_001157751.1:p.Tyr152Cys
NM_001164280.2:c.674A>G	NP_001157752.1:p.Tyr225Cys
NM_001467.6:c.674A>G	NP_001458.1:p.Tyr225Cys
NM_001164277.2:c.674A>G MANE Select	NP_001157749.1:p.Tyr225Cys