Canonical Allele Identifier: CA274441
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 189162
ClinVar RCV Id: RCV000169589
dbSNP Id: rs786204740

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119029369T>C , CM000673.2:g.119029369T>C GRCh38
NC_000011.9:g.118900079T>C , CM000673.1:g.118900079T>C GRCh37
NC_000011.8:g.118405289T>C NCBI36
NG_013331.1:g.6538A>G , LRG_187:g.6538A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000638186.1:n.304A>G
ENST00000638360.1:n.238A>G
ENST00000638925.1:n.237A>G
ENST00000650539.1:n.406A>G
ENST00000330775.9:c.1A>G
ENST00000357590.9:c.1A>G
ENST00000524428.5:n.1A>G
ENST00000525039.5:n.424A>G
ENST00000525102.5:n.758A>G
ENST00000525372.5:n.1A>G
ENST00000525787.1:n.296A>G
ENST00000526626.6:n.196A>G
ENST00000527992.5:n.228A>G
ENST00000529510.5:n.19A>G
ENST00000530407.5:n.197+23A>G
ENST00000532085.1:n.1495A>G
ENST00000532888.6:n.196A>G
ENST00000534384.1:n.221A>G
ENST00000538950.5:c.-172+23A>G ENSP00000475991.2:p.=
ENST00000545985.5:c.1A>G
NM_001164277.1:c.1A>G , LRG_187t1:c.1A>G
NM_001164278.1:c.1A>G
NM_001164279.1:c.-172+23A>G NP_001157751.1:p.=
NM_001164280.1:c.1A>G
NM_001467.5:c.1A>G
NM_001164278.2:c.1A>G
NM_001164279.2:c.-172+23A>G NP_001157751.1:p.=
NM_001164280.2:c.1A>G
NM_001467.6:c.1A>G
NM_001164277.2:c.1A>G