Canonical Allele Identifier: CA382901882

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118898352G>T (hg19) ; chr11:g.119027642G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027642G>T , CM000673.2:g.119027642G>T	GRCh38
NC_000011.9:g.118898352G>T , CM000673.1:g.118898352G>T	GRCh37
NC_000011.8:g.118403562G>T	NCBI36
NG_013331.1:g.8264C>A , LRG_187:g.8264C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.841C>A
ENST00000697845.1:n.765C>A
ENST00000697846.1:n.841C>A
ENST00000697847.1:n.841C>A
ENST00000697848.1:n.841C>A
ENST00000697849.1:n.1880C>A
ENST00000697850.1:n.841C>A
ENST00000697851.1:n.2201C>A
ENST00000638186.1:n.915C>A
ENST00000638360.1:n.747C>A
ENST00000638925.1:n.848C>A
ENST00000650539.1:n.1017C>A
ENST00000330775.9:c.611C>A	ENSP00000476242.2:p.Ser204Tyr
ENST00000357590.9:c.611C>A	ENSP00000476176.2:p.Ser204Tyr
ENST00000524428.5:n.933C>A
ENST00000525039.5:n.1035C>A
ENST00000525102.5:n.1369C>A
ENST00000525372.5:n.612C>A
ENST00000526275.5:n.1393C>A
ENST00000526626.6:n.574C>A
ENST00000527992.5:n.839C>A
ENST00000529510.5:n.400-547C>A
ENST00000530407.5:n.761C>A
ENST00000532085.1:n.3222C>A
ENST00000532888.6:n.907C>A
ENST00000538950.5:c.392C>A	ENSP00000475991.2:p.Ser131Tyr
ENST00000545985.5:c.611C>A	ENSP00000475241.2:p.Ser204Tyr
NM_001164277.1:c.611C>A , LRG_187t1:c.611C>A	NP_001157749.1:p.Ser204Tyr
NM_001164278.1:c.611C>A	NP_001157750.1:p.Ser204Tyr
NM_001164279.1:c.392C>A	NP_001157751.1:p.Ser131Tyr
NM_001164280.1:c.611C>A	NP_001157752.1:p.Ser204Tyr
NM_001467.5:c.611C>A	NP_001458.1:p.Ser204Tyr
NM_001164278.2:c.611C>A	NP_001157750.1:p.Ser204Tyr
NM_001164279.2:c.392C>A	NP_001157751.1:p.Ser131Tyr
NM_001164280.2:c.611C>A	NP_001157752.1:p.Ser204Tyr
NM_001467.6:c.611C>A	NP_001458.1:p.Ser204Tyr
NM_001164277.2:c.611C>A MANE Select	NP_001157749.1:p.Ser204Tyr