Canonical Allele Identifier: CA6311737

Gene: SLC37A4

Linked Data

• dbSNP Id: rs782117560
• ExAC: 11:118897614 T / C
• gnomAD v2: 11-118897614-T-C
• gnomAD v4: 11-119026904-T-C
• MyVariant Identifiers: chr11:g.118897614T>C (hg19) ; chr11:g.119026904T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026904T>C , CM000673.2:g.119026904T>C	GRCh38
NC_000011.9:g.118897614T>C , CM000673.1:g.118897614T>C	GRCh37
NC_000011.8:g.118402824T>C	NCBI36
NG_013331.1:g.9002A>G , LRG_187:g.9002A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1014+33A>G
ENST00000697845.1:n.971A>G
ENST00000697846.1:n.1014+33A>G
ENST00000697847.1:n.1014+33A>G
ENST00000697848.1:n.1014+33A>G
ENST00000697849.1:n.2086A>G
ENST00000697850.1:n.1014+33A>G
ENST00000697851.1:n.2407A>G
ENST00000638186.1:n.1088+33A>G
ENST00000638360.1:n.920+33A>G
ENST00000638925.1:n.1021+33A>G
ENST00000650539.1:n.1190+33A>G
ENST00000330775.9:c.784+33A>G	ENSP00000476242.2:n.784+33A>G
ENST00000357590.9:c.784+33A>G	ENSP00000476176.2:n.784+33A>G
ENST00000524428.5:n.1106+33A>G
ENST00000525039.5:n.1208+33A>G
ENST00000525102.5:n.1542+33A>G
ENST00000525372.5:n.785+33A>G
ENST00000526275.5:n.1566+33A>G
ENST00000527992.5:n.1012+33A>G
ENST00000529510.5:n.558+33A>G
ENST00000530407.5:n.934+33A>G
ENST00000532085.1:n.3428A>G
ENST00000532888.6:n.1113A>G
ENST00000538950.5:c.565+33A>G	ENSP00000475991.2:n.565+33A>G
ENST00000545985.5:c.784+33A>G	ENSP00000475241.2:n.784+33A>G
NM_001164277.1:c.784+33A>G , LRG_187t1:c.784+33A>G	NP_001157749.1:n.784+33A>G
NM_001164278.1:c.784+33A>G	NP_001157750.1:n.784+33A>G
NM_001164279.1:c.565+33A>G	NP_001157751.1:n.565+33A>G
NM_001164280.1:c.784+33A>G	NP_001157752.1:n.784+33A>G
NM_001467.5:c.784+33A>G	NP_001458.1:n.784+33A>G
NM_001164278.2:c.784+33A>G	NP_001157750.1:n.784+33A>G
NM_001164279.2:c.565+33A>G	NP_001157751.1:n.565+33A>G
NM_001164280.2:c.784+33A>G	NP_001157752.1:n.784+33A>G
NM_001467.6:c.784+33A>G	NP_001458.1:n.784+33A>G
NM_001164277.2:c.784+33A>G MANE Select	NP_001157749.1:n.784+33A>G