Canonical Allele Identifier: CA382899879

Gene: SLC37A4

Linked Data

• ClinVar Variation Id: 2017762
• ClinVar RCV Id: RCV002835308
• dbSNP Id: rs1943574435
• gnomAD v4: 11-119026602-C-T
• MyVariant Identifiers: chr11:g.118897312C>T (hg19) ; chr11:g.119026602C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026602C>T , CM000673.2:g.119026602C>T	GRCh38
NC_000011.9:g.118897312C>T , CM000673.1:g.118897312C>T	GRCh37
NC_000011.8:g.118402522C>T	NCBI36
NG_013331.1:g.9304G>A , LRG_187:g.9304G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1014+335G>A
ENST00000697845.1:n.1273G>A
ENST00000697846.1:n.1014+335G>A
ENST00000697847.1:n.1101G>A
ENST00000697848.1:n.1100+1G>A
ENST00000697849.1:n.2388G>A
ENST00000697850.1:n.1100+1G>A
ENST00000697851.1:n.2708+1G>A
ENST00000638186.1:n.1174+1G>A
ENST00000638360.1:n.1006+1G>A
ENST00000638925.1:n.1108G>A
ENST00000650539.1:n.1276+1G>A
ENST00000330775.9:c.870+1G>A	ENSP00000476242.2:n.870+1G>A
ENST00000357590.9:c.870+1G>A	ENSP00000476176.2:n.870+1G>A
ENST00000524428.5:n.1106+335G>A
ENST00000525039.5:n.1294+1G>A
ENST00000525102.5:n.1628+1G>A
ENST00000525372.5:n.872G>A
ENST00000526275.5:n.1652+1G>A
ENST00000527992.5:n.1098+1G>A
ENST00000529510.5:n.558+335G>A
ENST00000530407.5:n.1020+1G>A
ENST00000532085.1:n.3730G>A
ENST00000538950.5:c.651+1G>A	ENSP00000475991.2:n.651+1G>A
ENST00000545985.5:c.870+1G>A	ENSP00000475241.2:n.870+1G>A
NM_001164277.1:c.870+1G>A , LRG_187t1:c.870+1G>A	NP_001157749.1:n.870+1G>A
NM_001164278.1:c.870+1G>A	NP_001157750.1:n.870+1G>A
NM_001164279.1:c.651+1G>A	NP_001157751.1:n.651+1G>A
NM_001164280.1:c.870+1G>A	NP_001157752.1:n.870+1G>A
NM_001467.5:c.870+1G>A	NP_001458.1:n.870+1G>A
NM_001164278.2:c.870+1G>A	NP_001157750.1:n.870+1G>A
NM_001164279.2:c.651+1G>A	NP_001157751.1:n.651+1G>A
NM_001164280.2:c.870+1G>A	NP_001157752.1:n.870+1G>A
NM_001467.6:c.870+1G>A	NP_001458.1:n.870+1G>A
NM_001164277.2:c.870+1G>A MANE Select	NP_001157749.1:n.870+1G>A