Canonical Allele Identifier: CA382896966

Gene: SLC37A4

Linked Data

• dbSNP Id: rs2134630338
• MyVariant Identifiers: chr11:g.118896457A>G (hg19) ; chr11:g.119025747A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025747A>G , CM000673.2:g.119025747A>G	GRCh38
NC_000011.9:g.118896457A>G , CM000673.1:g.118896457A>G	GRCh37
NC_000011.8:g.118401667A>G	NCBI36
NG_013331.1:g.10159T>C , LRG_187:g.10159T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1139T>C
ENST00000697845.1:n.2128T>C
ENST00000697846.1:n.1139T>C
ENST00000697847.1:n.1212T>C
ENST00000697848.1:n.1225T>C
ENST00000697849.1:n.3243T>C
ENST00000697850.1:n.1434T>C
ENST00000697851.1:n.2822+220T>C
ENST00000638186.1:n.1288+220T>C
ENST00000638360.1:n.1120+220T>C
ENST00000638925.1:n.1253+220T>C
ENST00000650539.1:n.1401T>C
ENST00000330775.9:c.984+220T>C	ENSP00000476242.2:n.984+220T>C
ENST00000357590.9:c.995T>C	ENSP00000476176.2:p.Phe332Ser
ENST00000524428.5:n.1220+220T>C
ENST00000525039.5:n.1419T>C
ENST00000525102.5:n.1742+220T>C
ENST00000525372.5:n.1082+220T>C
ENST00000526275.5:n.1766+220T>C
ENST00000527992.5:n.1212+220T>C
ENST00000529510.5:n.672+220T>C
ENST00000530407.5:n.1134+220T>C
ENST00000532085.1:n.4585T>C
ENST00000538950.5:c.765+220T>C	ENSP00000475991.2:n.765+220T>C
ENST00000545985.5:c.984+220T>C	ENSP00000475241.2:n.984+220T>C
NM_001164277.1:c.984+220T>C , LRG_187t1:c.984+220T>C	NP_001157749.1:n.984+220T>C
NM_001164278.1:c.995T>C	NP_001157750.1:p.Phe332Ser
NM_001164279.1:c.765+220T>C	NP_001157751.1:n.765+220T>C
NM_001164280.1:c.984+220T>C	NP_001157752.1:n.984+220T>C
NM_001467.5:c.984+220T>C	NP_001458.1:n.984+220T>C
NM_001164278.2:c.995T>C	NP_001157750.1:p.Phe332Ser
NM_001164279.2:c.765+220T>C	NP_001157751.1:n.765+220T>C
NM_001164280.2:c.984+220T>C	NP_001157752.1:n.984+220T>C
NM_001467.6:c.984+220T>C	NP_001458.1:n.984+220T>C
NM_001164277.2:c.984+220T>C MANE Select	NP_001157749.1:n.984+220T>C