Canonical Allele Identifier: CA2616334698

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119026525-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026525T>C , CM000673.2:g.119026525T>C	GRCh38
NC_000011.9:g.118897235T>C , CM000673.1:g.118897235T>C	GRCh37
NC_000011.8:g.118402445T>C	NCBI36
NG_013331.1:g.9381A>G , LRG_187:g.9381A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+412A>G
ENST00000697845.1:n.1350A>G
ENST00000697846.1:n.1014+412A>G
ENST00000697847.1:n.1178A>G
ENST00000697848.1:n.1100+78A>G
ENST00000697849.1:n.2465A>G
ENST00000697850.1:n.1100+78A>G
ENST00000697851.1:n.2708+78A>G
ENST00000638186.1:n.1174+78A>G
ENST00000638360.1:n.1006+78A>G
ENST00000638925.1:n.1139+46A>G
ENST00000650539.1:n.1276+78A>G
ENST00000330775.9:c.870+78A>G	ENSP00000476242.2:n.870+78A>G
ENST00000357590.9:c.870+78A>G	ENSP00000476176.2:n.870+78A>G
ENST00000524428.5:n.1106+412A>G
ENST00000525039.5:n.1294+78A>G
ENST00000525102.5:n.1628+78A>G
ENST00000525372.5:n.949A>G
ENST00000526275.5:n.1652+78A>G
ENST00000527992.5:n.1098+78A>G
ENST00000529510.5:n.558+412A>G
ENST00000530407.5:n.1020+78A>G
ENST00000532085.1:n.3807A>G
ENST00000538950.5:c.651+78A>G	ENSP00000475991.2:n.651+78A>G
ENST00000545985.5:c.870+78A>G	ENSP00000475241.2:n.870+78A>G
NM_001164277.1:c.870+78A>G , LRG_187t1:c.870+78A>G	NP_001157749.1:n.870+78A>G
NM_001164278.1:c.870+78A>G	NP_001157750.1:n.870+78A>G
NM_001164279.1:c.651+78A>G	NP_001157751.1:n.651+78A>G
NM_001164280.1:c.870+78A>G	NP_001157752.1:n.870+78A>G
NM_001467.5:c.870+78A>G	NP_001458.1:n.870+78A>G
NM_001164278.2:c.870+78A>G	NP_001157750.1:n.870+78A>G
NM_001164279.2:c.651+78A>G	NP_001157751.1:n.651+78A>G
NM_001164280.2:c.870+78A>G	NP_001157752.1:n.870+78A>G
NM_001467.6:c.870+78A>G	NP_001458.1:n.870+78A>G
NM_001164277.2:c.870+78A>G MANE Select	NP_001157749.1:n.870+78A>G