Canonical Allele Identifier: CA229601322

Gene: SLC37A4

Linked Data

• dbSNP Id: rs899153871
• gnomAD v3: 11-119029432-C-T
• gnomAD v4: 11-119029432-C-T
• MyVariant Identifiers: chr11:g.118900142C>T (hg19) ; chr11:g.119029432C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029432C>T , CM000673.2:g.119029432C>T	GRCh38
NC_000011.9:g.118900142C>T , CM000673.1:g.118900142C>T	GRCh37
NC_000011.8:g.118405352C>T	NCBI36
NG_013331.1:g.6475G>A , LRG_187:g.6475G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.167G>A
ENST00000697846.1:n.167G>A
ENST00000697847.1:n.167G>A
ENST00000697848.1:n.167G>A
ENST00000697849.1:n.411G>A
ENST00000697850.1:n.167G>A
ENST00000697851.1:n.411G>A
ENST00000638186.1:n.241G>A
ENST00000638360.1:n.175G>A
ENST00000638925.1:n.174G>A
ENST00000650539.1:n.343G>A
ENST00000330775.9:c.-63G>A	ENSP00000476242.2:n.-63G>A
ENST00000357590.9:c.-63G>A	ENSP00000476176.2:n.-63G>A
ENST00000525039.5:n.361G>A
ENST00000525102.5:n.695G>A
ENST00000525787.1:n.233G>A
ENST00000526626.6:n.133G>A
ENST00000527992.5:n.165G>A
ENST00000530407.5:n.157G>A
ENST00000532085.1:n.1432G>A
ENST00000532888.6:n.133G>A
ENST00000534384.1:n.158G>A
ENST00000538950.5:c.-212G>A	ENSP00000475991.2:n.-212G>A
ENST00000545985.5:c.-63G>A	ENSP00000475241.2:n.-63G>A
NM_001164277.1:c.-63G>A , LRG_187t1:c.-63G>A	NP_001157749.1:n.-63G>A
NM_001164278.1:c.-63G>A	NP_001157750.1:n.-63G>A
NM_001164279.1:c.-212G>A	NP_001157751.1:n.-212G>A
NM_001164280.1:c.-63G>A	NP_001157752.1:n.-63G>A
NM_001467.5:c.-63G>A	NP_001458.1:n.-63G>A
NM_001164278.2:c.-63G>A	NP_001157750.1:n.-63G>A
NM_001164279.2:c.-212G>A	NP_001157751.1:n.-212G>A
NM_001164280.2:c.-63G>A	NP_001157752.1:n.-63G>A
NM_001467.6:c.-63G>A	NP_001458.1:n.-63G>A
NM_001164277.2:c.-63G>A MANE Select	NP_001157749.1:n.-63G>A