Canonical Allele Identifier: CA382908562

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118900003A>C (hg19) ; chr11:g.119029293A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029293A>C , CM000673.2:g.119029293A>C	GRCh38
NC_000011.9:g.118900003A>C , CM000673.1:g.118900003A>C	GRCh37
NC_000011.8:g.118405213A>C	NCBI36
NG_013331.1:g.6614T>G , LRG_187:g.6614T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.306T>G
ENST00000697846.1:n.306T>G
ENST00000697847.1:n.306T>G
ENST00000697848.1:n.306T>G
ENST00000697849.1:n.550T>G
ENST00000697850.1:n.306T>G
ENST00000697851.1:n.550T>G
ENST00000638186.1:n.380T>G
ENST00000638360.1:n.314T>G
ENST00000638925.1:n.313T>G
ENST00000650539.1:n.482T>G
ENST00000330775.9:c.77T>G	ENSP00000476242.2:p.Phe26Cys
ENST00000357590.9:c.77T>G	ENSP00000476176.2:p.Phe26Cys
ENST00000524428.5:n.77T>G
ENST00000525039.5:n.500T>G
ENST00000525102.5:n.834T>G
ENST00000525372.5:n.77T>G
ENST00000525787.1:n.372T>G
ENST00000526626.6:n.272T>G
ENST00000527992.5:n.304T>G
ENST00000529510.5:n.95T>G
ENST00000530407.5:n.197+99T>G
ENST00000532085.1:n.1571T>G
ENST00000532888.6:n.272T>G
ENST00000534384.1:n.297T>G
ENST00000538950.5:c.-172+99T>G	ENSP00000475991.2:n.-172+99T>G
ENST00000545985.5:c.77T>G	ENSP00000475241.2:p.Phe26Cys
NM_001164277.1:c.77T>G , LRG_187t1:c.77T>G	NP_001157749.1:p.Phe26Cys
NM_001164278.1:c.77T>G	NP_001157750.1:p.Phe26Cys
NM_001164279.1:c.-172+99T>G	NP_001157751.1:n.-172+99T>G
NM_001164280.1:c.77T>G	NP_001157752.1:p.Phe26Cys
NM_001467.5:c.77T>G	NP_001458.1:p.Phe26Cys
NM_001164278.2:c.77T>G	NP_001157750.1:p.Phe26Cys
NM_001164279.2:c.-172+99T>G	NP_001157751.1:n.-172+99T>G
NM_001164280.2:c.77T>G	NP_001157752.1:p.Phe26Cys
NM_001467.6:c.77T>G	NP_001458.1:p.Phe26Cys
NM_001164277.2:c.77T>G MANE Select	NP_001157749.1:p.Phe26Cys