Canonical Allele Identifier: CA477124948

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118896692G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025982G>C , CM000673.2:g.119025982G>C	GRCh38
NC_000011.9:g.118896692G>C , CM000673.1:g.118896692G>C	GRCh37
NC_000011.8:g.118401902G>C	NCBI36
NG_013331.1:g.9924C>G , LRG_187:g.9924C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1113C>G
ENST00000697845.1:n.1893C>G
ENST00000697846.1:n.1113C>G
ENST00000697847.1:n.1202-225C>G
ENST00000697848.1:n.1199C>G
ENST00000697849.1:n.3008C>G
ENST00000697850.1:n.1199C>G
ENST00000697851.1:n.2807C>G
ENST00000638186.1:n.1273C>G
ENST00000638360.1:n.1105C>G
ENST00000638925.1:n.1238C>G
ENST00000650539.1:n.1375C>G
ENST00000330775.9:c.969C>G	ENSP00000476242.2:p.Thr323=
ENST00000357590.9:c.969C>G	ENSP00000476176.2:p.Thr323=
ENST00000524428.5:n.1205C>G
ENST00000525039.5:n.1393C>G
ENST00000525102.5:n.1727C>G
ENST00000525372.5:n.1067C>G
ENST00000526275.5:n.1751C>G
ENST00000527992.5:n.1197C>G
ENST00000529510.5:n.657C>G
ENST00000530407.5:n.1119C>G
ENST00000532085.1:n.4350C>G
ENST00000538950.5:c.750C>G	ENSP00000475991.2:p.Thr250=
ENST00000545985.5:c.969C>G	ENSP00000475241.2:p.Thr323=
NM_001164277.1:c.969C>G , LRG_187t1:c.969C>G	NP_001157749.1:p.Thr323=
NM_001164278.1:c.969C>G	NP_001157750.1:p.Thr323=
NM_001164279.1:c.750C>G	NP_001157751.1:p.Thr250=
NM_001164280.1:c.969C>G	NP_001157752.1:p.Thr323=
NM_001467.5:c.969C>G	NP_001458.1:p.Thr323=
NM_001164278.2:c.969C>G	NP_001157750.1:p.Thr323=
NM_001164279.2:c.750C>G	NP_001157751.1:p.Thr250=
NM_001164280.2:c.969C>G	NP_001157752.1:p.Thr323=
NM_001467.6:c.969C>G	NP_001458.1:p.Thr323=
NM_001164277.2:c.969C>G MANE Select	NP_001157749.1:p.Thr323=