Canonical Allele Identifier: CA2616334739

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119026564-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026564A>C , CM000673.2:g.119026564A>C	GRCh38
NC_000011.9:g.118897274A>C , CM000673.1:g.118897274A>C	GRCh37
NC_000011.8:g.118402484A>C	NCBI36
NG_013331.1:g.9342T>G , LRG_187:g.9342T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+373T>G
ENST00000697845.1:n.1311T>G
ENST00000697846.1:n.1014+373T>G
ENST00000697847.1:n.1139T>G
ENST00000697848.1:n.1100+39T>G
ENST00000697849.1:n.2426T>G
ENST00000697850.1:n.1100+39T>G
ENST00000697851.1:n.2708+39T>G
ENST00000638186.1:n.1174+39T>G
ENST00000638360.1:n.1006+39T>G
ENST00000638925.1:n.1139+7T>G
ENST00000650539.1:n.1276+39T>G
ENST00000330775.9:c.870+39T>G	ENSP00000476242.2:n.870+39T>G
ENST00000357590.9:c.870+39T>G	ENSP00000476176.2:n.870+39T>G
ENST00000524428.5:n.1106+373T>G
ENST00000525039.5:n.1294+39T>G
ENST00000525102.5:n.1628+39T>G
ENST00000525372.5:n.910T>G
ENST00000526275.5:n.1652+39T>G
ENST00000527992.5:n.1098+39T>G
ENST00000529510.5:n.558+373T>G
ENST00000530407.5:n.1020+39T>G
ENST00000532085.1:n.3768T>G
ENST00000538950.5:c.651+39T>G	ENSP00000475991.2:n.651+39T>G
ENST00000545985.5:c.870+39T>G	ENSP00000475241.2:n.870+39T>G
NM_001164277.1:c.870+39T>G , LRG_187t1:c.870+39T>G	NP_001157749.1:n.870+39T>G
NM_001164278.1:c.870+39T>G	NP_001157750.1:n.870+39T>G
NM_001164279.1:c.651+39T>G	NP_001157751.1:n.651+39T>G
NM_001164280.1:c.870+39T>G	NP_001157752.1:n.870+39T>G
NM_001467.5:c.870+39T>G	NP_001458.1:n.870+39T>G
NM_001164278.2:c.870+39T>G	NP_001157750.1:n.870+39T>G
NM_001164279.2:c.651+39T>G	NP_001157751.1:n.651+39T>G
NM_001164280.2:c.870+39T>G	NP_001157752.1:n.870+39T>G
NM_001467.6:c.870+39T>G	NP_001458.1:n.870+39T>G
NM_001164277.2:c.870+39T>G MANE Select	NP_001157749.1:n.870+39T>G