Canonical Allele Identifier: CA2575003402

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119028781-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028781A>G , CM000673.2:g.119028781A>G	GRCh38
NC_000011.9:g.118899491A>G , CM000673.1:g.118899491A>G	GRCh37
NC_000011.8:g.118404701A>G	NCBI36
NG_013331.1:g.7126T>C , LRG_187:g.7126T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.378-355T>C
ENST00000697846.1:n.378-355T>C
ENST00000697847.1:n.378-355T>C
ENST00000697848.1:n.378-355T>C
ENST00000697849.1:n.1062T>C
ENST00000697850.1:n.378-355T>C
ENST00000697851.1:n.1062T>C
ENST00000638186.1:n.452-355T>C
ENST00000638360.1:n.386-355T>C
ENST00000638925.1:n.385-355T>C
ENST00000650539.1:n.554-355T>C
ENST00000330775.9:c.149-355T>C	ENSP00000476242.2:n.149-355T>C
ENST00000357590.9:c.149-355T>C	ENSP00000476176.2:n.149-355T>C
ENST00000524428.5:n.149-355T>C
ENST00000525039.5:n.572-355T>C
ENST00000525102.5:n.906-355T>C
ENST00000525372.5:n.149-355T>C
ENST00000525787.1:n.444-355T>C
ENST00000526275.5:n.254T>C
ENST00000526626.6:n.343+441T>C
ENST00000527992.5:n.376-355T>C
ENST00000529510.5:n.167-355T>C
ENST00000530407.5:n.251T>C
ENST00000532085.1:n.2083T>C
ENST00000532888.6:n.397T>C
ENST00000534384.1:n.369-355T>C
ENST00000538950.5:c.-118T>C	ENSP00000475991.2:n.-118T>C
ENST00000545985.5:c.149-355T>C	ENSP00000475241.2:n.149-355T>C
NM_001164277.1:c.149-355T>C , LRG_187t1:c.149-355T>C	NP_001157749.1:n.149-355T>C
NM_001164278.1:c.149-355T>C	NP_001157750.1:n.149-355T>C
NM_001164279.1:c.-118T>C	NP_001157751.1:n.-118T>C
NM_001164280.1:c.149-355T>C	NP_001157752.1:n.149-355T>C
NM_001467.5:c.149-355T>C	NP_001458.1:n.149-355T>C
NM_001164278.2:c.149-355T>C	NP_001157750.1:n.149-355T>C
NM_001164279.2:c.-118T>C	NP_001157751.1:n.-118T>C
NM_001164280.2:c.149-355T>C	NP_001157752.1:n.149-355T>C
NM_001467.6:c.149-355T>C	NP_001458.1:n.149-355T>C
NM_001164277.2:c.149-355T>C MANE Select	NP_001157749.1:n.149-355T>C