Canonical Allele Identifier: CA229601460

Gene: SLC37A4

Linked Data

• dbSNP Id: rs782597725
• gnomAD v2: 11-118900198-C-G
• gnomAD v4: 11-119029488-C-G
• MyVariant Identifiers: chr11:g.118900198C>G (hg19) ; chr11:g.119029488C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029488C>G , CM000673.2:g.119029488C>G	GRCh38
NC_000011.9:g.118900198C>G , CM000673.1:g.118900198C>G	GRCh37
NC_000011.8:g.118405408C>G	NCBI36
NG_013331.1:g.6419G>C , LRG_187:g.6419G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.111G>C
ENST00000697846.1:n.111G>C
ENST00000697847.1:n.111G>C
ENST00000697848.1:n.111G>C
ENST00000697849.1:n.355G>C
ENST00000697850.1:n.111G>C
ENST00000697851.1:n.355G>C
ENST00000638186.1:n.185G>C
ENST00000638360.1:n.119G>C
ENST00000638925.1:n.118G>C
ENST00000650539.1:n.287G>C
ENST00000330775.9:c.-119G>C	ENSP00000476242.2:n.-119G>C
ENST00000357590.9:c.-119G>C	ENSP00000476176.2:n.-119G>C
ENST00000525039.5:n.305G>C
ENST00000525102.5:n.639G>C
ENST00000525787.1:n.177G>C
ENST00000526626.6:n.77G>C
ENST00000527992.5:n.109G>C
ENST00000530407.5:n.101G>C
ENST00000532085.1:n.1376G>C
ENST00000532888.6:n.77G>C
ENST00000534384.1:n.102G>C
ENST00000538950.5:c.-268G>C	ENSP00000475991.2:n.-268G>C
ENST00000545985.5:c.-119G>C	ENSP00000475241.2:n.-119G>C
NM_001164277.1:c.-119G>C , LRG_187t1:c.-119G>C	NP_001157749.1:n.-119G>C
NM_001164278.1:c.-119G>C	NP_001157750.1:n.-119G>C
NM_001164279.1:c.-268G>C	NP_001157751.1:n.-268G>C
NM_001164280.1:c.-119G>C	NP_001157752.1:n.-119G>C
NM_001467.5:c.-119G>C	NP_001458.1:n.-119G>C
NM_001164278.2:c.-119G>C	NP_001157750.1:n.-119G>C
NM_001164279.2:c.-268G>C	NP_001157751.1:n.-268G>C
NM_001467.6:c.-119G>C	NP_001458.1:n.-119G>C
NM_001164277.2:c.-119G>C MANE Select	NP_001157749.1:n.-119G>C