Canonical Allele Identifier: CA229600397

Gene: SLC37A4

Linked Data

• dbSNP Id: rs140756683
• gnomAD v2: 11-118899529-A-T
• gnomAD v3: 11-119028819-A-T
• gnomAD v4: 11-119028819-A-T
• MyVariant Identifiers: chr11:g.118899529A>T (hg19) ; chr11:g.119028819A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028819A>T , CM000673.2:g.119028819A>T	GRCh38
NC_000011.9:g.118899529A>T , CM000673.1:g.118899529A>T	GRCh37
NC_000011.8:g.118404739A>T	NCBI36
NG_013331.1:g.7088T>A , LRG_187:g.7088T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.378-393T>A
ENST00000697846.1:n.378-393T>A
ENST00000697847.1:n.378-393T>A
ENST00000697848.1:n.378-393T>A
ENST00000697849.1:n.1024T>A
ENST00000697850.1:n.378-393T>A
ENST00000697851.1:n.1024T>A
ENST00000638186.1:n.452-393T>A
ENST00000638360.1:n.386-393T>A
ENST00000638925.1:n.385-393T>A
ENST00000650539.1:n.554-393T>A
ENST00000330775.9:c.149-393T>A	ENSP00000476242.2:n.149-393T>A
ENST00000357590.9:c.149-393T>A	ENSP00000476176.2:n.149-393T>A
ENST00000524428.5:n.149-393T>A
ENST00000525039.5:n.572-393T>A
ENST00000525102.5:n.906-393T>A
ENST00000525372.5:n.149-393T>A
ENST00000525787.1:n.444-393T>A
ENST00000526275.5:n.216T>A
ENST00000526626.6:n.343+403T>A
ENST00000527992.5:n.376-393T>A
ENST00000529510.5:n.167-393T>A
ENST00000530407.5:n.213T>A
ENST00000532085.1:n.2045T>A
ENST00000532888.6:n.359T>A
ENST00000534384.1:n.369-393T>A
ENST00000538950.5:c.-156T>A	ENSP00000475991.2:n.-156T>A
ENST00000545985.5:c.149-393T>A	ENSP00000475241.2:n.149-393T>A
NM_001164277.1:c.149-393T>A , LRG_187t1:c.149-393T>A	NP_001157749.1:n.149-393T>A
NM_001164278.1:c.149-393T>A	NP_001157750.1:n.149-393T>A
NM_001164279.1:c.-156T>A	NP_001157751.1:n.-156T>A
NM_001164280.1:c.149-393T>A	NP_001157752.1:n.149-393T>A
NM_001467.5:c.149-393T>A	NP_001458.1:n.149-393T>A
NM_001164278.2:c.149-393T>A	NP_001157750.1:n.149-393T>A
NM_001164279.2:c.-156T>A	NP_001157751.1:n.-156T>A
NM_001164280.2:c.149-393T>A	NP_001157752.1:n.149-393T>A
NM_001467.6:c.149-393T>A	NP_001458.1:n.149-393T>A
NM_001164277.2:c.149-393T>A MANE Select	NP_001157749.1:n.149-393T>A