Canonical Allele Identifier: CA229598553

Gene: SLC37A4

Linked Data

• dbSNP Id: rs782200053
• gnomAD v3: 11-119027263-C-T
• gnomAD v4: 11-119027263-C-T
• MyVariant Identifiers: chr11:g.118897973C>T (hg19) ; chr11:g.119027263C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027263C>T , CM000673.2:g.119027263C>T	GRCh38
NC_000011.9:g.118897973C>T , CM000673.1:g.118897973C>T	GRCh37
NC_000011.8:g.118403183C>T	NCBI36
NG_013331.1:g.8643G>A , LRG_187:g.8643G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.856-168G>A
ENST00000697845.1:n.780-168G>A
ENST00000697846.1:n.856-168G>A
ENST00000697847.1:n.856-168G>A
ENST00000697848.1:n.856-168G>A
ENST00000697849.1:n.1895-168G>A
ENST00000697850.1:n.856-168G>A
ENST00000697851.1:n.2216-168G>A
ENST00000638186.1:n.930-168G>A
ENST00000638360.1:n.762-168G>A
ENST00000638925.1:n.863-168G>A
ENST00000650539.1:n.1032-168G>A
ENST00000330775.9:c.626-168G>A	ENSP00000476242.2:n.626-168G>A
ENST00000357590.9:c.626-168G>A	ENSP00000476176.2:n.626-168G>A
ENST00000524428.5:n.948-168G>A
ENST00000525039.5:n.1050-168G>A
ENST00000525102.5:n.1384-168G>A
ENST00000525372.5:n.627-168G>A
ENST00000526275.5:n.1408-168G>A
ENST00000526626.6:n.589-168G>A
ENST00000527992.5:n.854-168G>A
ENST00000529510.5:n.400-168G>A
ENST00000530407.5:n.776-168G>A
ENST00000532085.1:n.3237-168G>A
ENST00000532888.6:n.922-168G>A
ENST00000538950.5:c.407-168G>A	ENSP00000475991.2:n.407-168G>A
ENST00000545985.5:c.626-168G>A	ENSP00000475241.2:n.626-168G>A
NM_001164277.1:c.626-168G>A , LRG_187t1:c.626-168G>A	NP_001157749.1:n.626-168G>A
NM_001164278.1:c.626-168G>A	NP_001157750.1:n.626-168G>A
NM_001164279.1:c.407-168G>A	NP_001157751.1:n.407-168G>A
NM_001164280.1:c.626-168G>A	NP_001157752.1:n.626-168G>A
NM_001467.5:c.626-168G>A	NP_001458.1:n.626-168G>A
NM_001164278.2:c.626-168G>A	NP_001157750.1:n.626-168G>A
NM_001164279.2:c.407-168G>A	NP_001157751.1:n.407-168G>A
NM_001164280.2:c.626-168G>A	NP_001157752.1:n.626-168G>A
NM_001467.6:c.626-168G>A	NP_001458.1:n.626-168G>A
NM_001164277.2:c.626-168G>A MANE Select	NP_001157749.1:n.626-168G>A