Canonical Allele Identifier: CA672397593

Gene: SLC37A4

Linked Data

• dbSNP Id: rs1485326638
• gnomAD v3: 11-119029507-T-C
• gnomAD v4: 11-119029507-T-C
• MyVariant Identifiers: chr11:g.118900217T>C (hg19) ; chr11:g.119029507T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029507T>C , CM000673.2:g.119029507T>C	GRCh38
NC_000011.9:g.118900217T>C , CM000673.1:g.118900217T>C	GRCh37
NC_000011.8:g.118405427T>C	NCBI36
NG_013331.1:g.6400A>G , LRG_187:g.6400A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.92A>G
ENST00000697846.1:n.92A>G
ENST00000697847.1:n.92A>G
ENST00000697848.1:n.92A>G
ENST00000697849.1:n.336A>G
ENST00000697850.1:n.92A>G
ENST00000697851.1:n.336A>G
ENST00000638186.1:n.166A>G
ENST00000638360.1:n.100A>G
ENST00000638925.1:n.99A>G
ENST00000650539.1:n.268A>G
ENST00000330775.9:c.-138A>G	ENSP00000476242.2:n.-138A>G
ENST00000357590.9:c.-138A>G	ENSP00000476176.2:n.-138A>G
ENST00000525039.5:n.286A>G
ENST00000525102.5:n.620A>G
ENST00000525787.1:n.158A>G
ENST00000526626.6:n.58A>G
ENST00000527992.5:n.90A>G
ENST00000530407.5:n.82A>G
ENST00000532085.1:n.1357A>G
ENST00000532888.6:n.58A>G
ENST00000534384.1:n.83A>G
ENST00000538950.5:c.-287A>G	ENSP00000475991.2:n.-287A>G
ENST00000545985.5:c.-138A>G	ENSP00000475241.2:n.-138A>G
NM_001164277.1:c.-138A>G , LRG_187t1:c.-138A>G	NP_001157749.1:n.-138A>G
NM_001164278.1:c.-138A>G	NP_001157750.1:n.-138A>G
NM_001164279.1:c.-287A>G	NP_001157751.1:n.-287A>G
NM_001164280.1:c.-138A>G	NP_001157752.1:n.-138A>G
NM_001467.5:c.-138A>G	NP_001458.1:n.-138A>G
NM_001164278.2:c.-138A>G	NP_001157750.1:n.-138A>G
NM_001164279.2:c.-287A>G	NP_001157751.1:n.-287A>G
NM_001467.6:c.-138A>G	NP_001458.1:n.-138A>G
NM_001164277.2:c.-138A>G MANE Select	NP_001157749.1:n.-138A>G