Canonical Allele Identifier: CA477125303

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118897343A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026633A>C , CM000673.2:g.119026633A>C	GRCh38
NC_000011.9:g.118897343A>C , CM000673.1:g.118897343A>C	GRCh37
NC_000011.8:g.118402553A>C	NCBI36
NG_013331.1:g.9273T>G , LRG_187:g.9273T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+304T>G
ENST00000697845.1:n.1242T>G
ENST00000697846.1:n.1014+304T>G
ENST00000697847.1:n.1070T>G
ENST00000697848.1:n.1070T>G
ENST00000697849.1:n.2357T>G
ENST00000697850.1:n.1070T>G
ENST00000697851.1:n.2678T>G
ENST00000638186.1:n.1144T>G
ENST00000638360.1:n.976T>G
ENST00000638925.1:n.1077T>G
ENST00000650539.1:n.1246T>G
ENST00000330775.9:c.840T>G	ENSP00000476242.2:p.Ala280=
ENST00000357590.9:c.840T>G	ENSP00000476176.2:p.Ala280=
ENST00000524428.5:n.1106+304T>G
ENST00000525039.5:n.1264T>G
ENST00000525102.5:n.1598T>G
ENST00000525372.5:n.841T>G
ENST00000526275.5:n.1622T>G
ENST00000527992.5:n.1068T>G
ENST00000529510.5:n.558+304T>G
ENST00000530407.5:n.990T>G
ENST00000532085.1:n.3699T>G
ENST00000538950.5:c.621T>G	ENSP00000475991.2:p.Ala207=
ENST00000545985.5:c.840T>G	ENSP00000475241.2:p.Ala280=
NM_001164277.1:c.840T>G , LRG_187t1:c.840T>G	NP_001157749.1:p.Ala280=
NM_001164278.1:c.840T>G	NP_001157750.1:p.Ala280=
NM_001164279.1:c.621T>G	NP_001157751.1:p.Ala207=
NM_001164280.1:c.840T>G	NP_001157752.1:p.Ala280=
NM_001467.5:c.840T>G	NP_001458.1:p.Ala280=
NM_001164278.2:c.840T>G	NP_001157750.1:p.Ala280=
NM_001164279.2:c.621T>G	NP_001157751.1:p.Ala207=
NM_001164280.2:c.840T>G	NP_001157752.1:p.Ala280=
NM_001467.6:c.840T>G	NP_001458.1:p.Ala280=
NM_001164277.2:c.840T>G MANE Select	NP_001157749.1:p.Ala280=