Canonical Allele Identifier: CA2616334531

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119026342-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026342G>T , CM000673.2:g.119026342G>T	GRCh38
NC_000011.9:g.118897052G>T , CM000673.1:g.118897052G>T	GRCh37
NC_000011.8:g.118402262G>T	NCBI36
NG_013331.1:g.9564C>A , LRG_187:g.9564C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1015-262C>A
ENST00000697845.1:n.1533C>A
ENST00000697846.1:n.1015-262C>A
ENST00000697847.1:n.1201+160C>A
ENST00000697848.1:n.1101-262C>A
ENST00000697849.1:n.2648C>A
ENST00000697850.1:n.1101-262C>A
ENST00000697851.1:n.2709-262C>A
ENST00000638186.1:n.1175-262C>A
ENST00000638360.1:n.1007-262C>A
ENST00000638925.1:n.1139+229C>A
ENST00000650539.1:n.1277-262C>A
ENST00000330775.9:c.871-262C>A	ENSP00000476242.2:n.871-262C>A
ENST00000357590.9:c.871-262C>A	ENSP00000476176.2:n.871-262C>A
ENST00000524428.5:n.1107-262C>A
ENST00000525039.5:n.1295-262C>A
ENST00000525102.5:n.1629-262C>A
ENST00000525372.5:n.968+164C>A
ENST00000526275.5:n.1653-262C>A
ENST00000527992.5:n.1099-262C>A
ENST00000529510.5:n.559-262C>A
ENST00000530407.5:n.1021-262C>A
ENST00000532085.1:n.3990C>A
ENST00000538950.5:c.652-262C>A	ENSP00000475991.2:n.652-262C>A
ENST00000545985.5:c.871-262C>A	ENSP00000475241.2:n.871-262C>A
NM_001164277.1:c.871-262C>A , LRG_187t1:c.871-262C>A	NP_001157749.1:n.871-262C>A
NM_001164278.1:c.871-262C>A	NP_001157750.1:n.871-262C>A
NM_001164279.1:c.652-262C>A	NP_001157751.1:n.652-262C>A
NM_001164280.1:c.871-262C>A	NP_001157752.1:n.871-262C>A
NM_001467.5:c.871-262C>A	NP_001458.1:n.871-262C>A
NM_001164278.2:c.871-262C>A	NP_001157750.1:n.871-262C>A
NM_001164279.2:c.652-262C>A	NP_001157751.1:n.652-262C>A
NM_001164280.2:c.871-262C>A	NP_001157752.1:n.871-262C>A
NM_001467.6:c.871-262C>A	NP_001458.1:n.871-262C>A
NM_001164277.2:c.871-262C>A MANE Select	NP_001157749.1:n.871-262C>A