Canonical Allele Identifier: CA382906447

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028405G>T , CM000673.2:g.119028405G>T	GRCh38
NC_000011.9:g.118899115G>T , CM000673.1:g.118899115G>T	GRCh37
NC_000011.8:g.118404325G>T	NCBI36
NG_013331.1:g.7502C>A , LRG_187:g.7502C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001164277.2:c.170C>A MANE Select	NP_001157749.1:p.Ser57Ter
NM_001164277.1:c.170C>A , LRG_187t1:c.170C>A	NP_001157749.1:p.Ser57Ter
NM_001164278.1:c.170C>A	NP_001157750.1:p.Ser57Ter
NM_001164278.2:c.170C>A	NP_001157750.1:p.Ser57Ter
NM_001164279.1:c.-50C>A	NP_001157751.1:n.-50C>A
NM_001164279.2:c.-50C>A	NP_001157751.1:n.-50C>A
NM_001164280.1:c.170C>A	NP_001157752.1:p.Ser57Ter
NM_001164280.2:c.170C>A	NP_001157752.1:p.Ser57Ter
NM_001467.5:c.170C>A	NP_001458.1:p.Ser57Ter
NM_001467.6:c.170C>A	NP_001458.1:p.Ser57Ter
ENST00000330775.9:c.170C>A	ENSP00000476242.2:p.Ser57Ter
ENST00000357590.9:c.170C>A	ENSP00000476176.2:p.Ser57Ter
ENST00000524428.5:n.170C>A
ENST00000525039.5:n.593C>A
ENST00000525102.5:n.927C>A
ENST00000525372.5:n.170C>A
ENST00000525787.1:n.465C>A
ENST00000526275.5:n.630C>A
ENST00000526626.6:n.344-533C>A
ENST00000527992.5:n.397C>A
ENST00000529510.5:n.188C>A
ENST00000529510.6:n.399C>A
ENST00000530407.5:n.319C>A
ENST00000532085.1:n.2459C>A
ENST00000532888.6:n.465C>A
ENST00000534384.1:n.390C>A
ENST00000538950.5:c.-50C>A	ENSP00000475991.2:n.-50C>A
ENST00000545985.5:c.170C>A	ENSP00000475241.2:p.Ser57Ter
ENST00000638186.1:n.473C>A
ENST00000638360.1:n.407C>A
ENST00000638925.1:n.406C>A
ENST00000650539.1:n.575C>A
ENST00000697845.1:n.323C>A
ENST00000697846.1:n.399C>A
ENST00000697847.1:n.399C>A
ENST00000697848.1:n.399C>A
ENST00000697849.1:n.1438C>A
ENST00000697850.1:n.399C>A
ENST00000697851.1:n.1438C>A