Canonical Allele Identifier: CA229601445

Gene: SLC37A4

Linked Data

• dbSNP Id: rs989625109
• gnomAD v3: 11-119029485-A-C
• gnomAD v4: 11-119029485-A-C
• MyVariant Identifiers: chr11:g.118900195A>C (hg19) ; chr11:g.119029485A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029485A>C , CM000673.2:g.119029485A>C	GRCh38
NC_000011.9:g.118900195A>C , CM000673.1:g.118900195A>C	GRCh37
NC_000011.8:g.118405405A>C	NCBI36
NG_013331.1:g.6422T>G , LRG_187:g.6422T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.114T>G
ENST00000697846.1:n.114T>G
ENST00000697847.1:n.114T>G
ENST00000697848.1:n.114T>G
ENST00000697849.1:n.358T>G
ENST00000697850.1:n.114T>G
ENST00000697851.1:n.358T>G
ENST00000638186.1:n.188T>G
ENST00000638360.1:n.122T>G
ENST00000638925.1:n.121T>G
ENST00000650539.1:n.290T>G
ENST00000330775.9:c.-116T>G	ENSP00000476242.2:n.-116T>G
ENST00000357590.9:c.-116T>G	ENSP00000476176.2:n.-116T>G
ENST00000525039.5:n.308T>G
ENST00000525102.5:n.642T>G
ENST00000525787.1:n.180T>G
ENST00000526626.6:n.80T>G
ENST00000527992.5:n.112T>G
ENST00000530407.5:n.104T>G
ENST00000532085.1:n.1379T>G
ENST00000532888.6:n.80T>G
ENST00000534384.1:n.105T>G
ENST00000538950.5:c.-265T>G	ENSP00000475991.2:n.-265T>G
ENST00000545985.5:c.-116T>G	ENSP00000475241.2:n.-116T>G
NM_001164277.1:c.-116T>G , LRG_187t1:c.-116T>G	NP_001157749.1:n.-116T>G
NM_001164278.1:c.-116T>G	NP_001157750.1:n.-116T>G
NM_001164279.1:c.-265T>G	NP_001157751.1:n.-265T>G
NM_001164280.1:c.-116T>G	NP_001157752.1:n.-116T>G
NM_001467.5:c.-116T>G	NP_001458.1:n.-116T>G
NM_001164278.2:c.-116T>G	NP_001157750.1:n.-116T>G
NM_001164279.2:c.-265T>G	NP_001157751.1:n.-265T>G
NM_001467.6:c.-116T>G	NP_001458.1:n.-116T>G
NM_001164277.2:c.-116T>G MANE Select	NP_001157749.1:n.-116T>G