Canonical Allele Identifier: CA2575003407

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028821G>C , CM000673.2:g.119028821G>C	GRCh38
NC_000011.9:g.118899531G>C , CM000673.1:g.118899531G>C	GRCh37
NC_000011.8:g.118404741G>C	NCBI36
NG_013331.1:g.7086C>G , LRG_187:g.7086C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.378-395C>G
ENST00000697846.1:n.378-395C>G
ENST00000697847.1:n.378-395C>G
ENST00000697848.1:n.378-395C>G
ENST00000697849.1:n.1022C>G
ENST00000697850.1:n.378-395C>G
ENST00000697851.1:n.1022C>G
ENST00000638186.1:n.452-395C>G
ENST00000638360.1:n.386-395C>G
ENST00000638925.1:n.385-395C>G
ENST00000650539.1:n.554-395C>G
ENST00000330775.9:c.149-395C>G	ENSP00000476242.2:n.149-395C>G
ENST00000357590.9:c.149-395C>G	ENSP00000476176.2:n.149-395C>G
ENST00000524428.5:n.149-395C>G
ENST00000525039.5:n.572-395C>G
ENST00000525102.5:n.906-395C>G
ENST00000525372.5:n.149-395C>G
ENST00000525787.1:n.444-395C>G
ENST00000526275.5:n.214C>G
ENST00000526626.6:n.343+401C>G
ENST00000527992.5:n.376-395C>G
ENST00000529510.5:n.167-395C>G
ENST00000530407.5:n.211C>G
ENST00000532085.1:n.2043C>G
ENST00000532888.6:n.357C>G
ENST00000534384.1:n.369-395C>G
ENST00000538950.5:c.-158C>G	ENSP00000475991.2:n.-158C>G
ENST00000545985.5:c.149-395C>G	ENSP00000475241.2:n.149-395C>G
NM_001164277.1:c.149-395C>G , LRG_187t1:c.149-395C>G	NP_001157749.1:n.149-395C>G
NM_001164278.1:c.149-395C>G	NP_001157750.1:n.149-395C>G
NM_001164279.1:c.-158C>G	NP_001157751.1:n.-158C>G
NM_001164280.1:c.149-395C>G	NP_001157752.1:n.149-395C>G
NM_001467.5:c.149-395C>G	NP_001458.1:n.149-395C>G
NM_001164278.2:c.149-395C>G	NP_001157750.1:n.149-395C>G
NM_001164279.2:c.-158C>G	NP_001157751.1:n.-158C>G
NM_001164280.2:c.149-395C>G	NP_001157752.1:n.149-395C>G
NM_001467.6:c.149-395C>G	NP_001458.1:n.149-395C>G
NM_001164277.2:c.149-395C>G MANE Select	NP_001157749.1:n.149-395C>G