Canonical Allele Identifier: CA382908544

Gene: SLC37A4

Linked Data

• dbSNP Id: rs1943675742
• MyVariant Identifiers: chr11:g.118900002G>T (hg19) ; chr11:g.119029292G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029292G>T , CM000673.2:g.119029292G>T	GRCh38
NC_000011.9:g.118900002G>T , CM000673.1:g.118900002G>T	GRCh37
NC_000011.8:g.118405212G>T	NCBI36
NG_013331.1:g.6615C>A , LRG_187:g.6615C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.307C>A
ENST00000697846.1:n.307C>A
ENST00000697847.1:n.307C>A
ENST00000697848.1:n.307C>A
ENST00000697849.1:n.551C>A
ENST00000697850.1:n.307C>A
ENST00000697851.1:n.551C>A
ENST00000638186.1:n.381C>A
ENST00000638360.1:n.315C>A
ENST00000638925.1:n.314C>A
ENST00000650539.1:n.483C>A
ENST00000330775.9:c.78C>A	ENSP00000476242.2:p.Phe26Leu
ENST00000357590.9:c.78C>A	ENSP00000476176.2:p.Phe26Leu
ENST00000524428.5:n.78C>A
ENST00000525039.5:n.501C>A
ENST00000525102.5:n.835C>A
ENST00000525372.5:n.78C>A
ENST00000525787.1:n.373C>A
ENST00000526626.6:n.273C>A
ENST00000527992.5:n.305C>A
ENST00000529510.5:n.96C>A
ENST00000530407.5:n.197+100C>A
ENST00000532085.1:n.1572C>A
ENST00000532888.6:n.273C>A
ENST00000534384.1:n.298C>A
ENST00000538950.5:c.-172+100C>A	ENSP00000475991.2:n.-172+100C>A
ENST00000545985.5:c.78C>A	ENSP00000475241.2:p.Phe26Leu
NM_001164277.1:c.78C>A , LRG_187t1:c.78C>A	NP_001157749.1:p.Phe26Leu
NM_001164278.1:c.78C>A	NP_001157750.1:p.Phe26Leu
NM_001164279.1:c.-172+100C>A	NP_001157751.1:n.-172+100C>A
NM_001164280.1:c.78C>A	NP_001157752.1:p.Phe26Leu
NM_001467.5:c.78C>A	NP_001458.1:p.Phe26Leu
NM_001164278.2:c.78C>A	NP_001157750.1:p.Phe26Leu
NM_001164279.2:c.-172+100C>A	NP_001157751.1:n.-172+100C>A
NM_001164280.2:c.78C>A	NP_001157752.1:p.Phe26Leu
NM_001467.6:c.78C>A	NP_001458.1:p.Phe26Leu
NM_001164277.2:c.78C>A MANE Select	NP_001157749.1:p.Phe26Leu