Canonical Allele Identifier: CA229601439

Gene: SLC37A4

Linked Data

• dbSNP Id: rs189829762
• gnomAD v2: 11-118900190-C-T
• gnomAD v3: 11-119029480-C-T
• gnomAD v4: 11-119029480-C-T
• MyVariant Identifiers: chr11:g.118900190C>T (hg19) ; chr11:g.119029480C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029480C>T , CM000673.2:g.119029480C>T	GRCh38
NC_000011.9:g.118900190C>T , CM000673.1:g.118900190C>T	GRCh37
NC_000011.8:g.118405400C>T	NCBI36
NG_013331.1:g.6427G>A , LRG_187:g.6427G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.119G>A
ENST00000697846.1:n.119G>A
ENST00000697847.1:n.119G>A
ENST00000697848.1:n.119G>A
ENST00000697849.1:n.363G>A
ENST00000697850.1:n.119G>A
ENST00000697851.1:n.363G>A
ENST00000638186.1:n.193G>A
ENST00000638360.1:n.127G>A
ENST00000638925.1:n.126G>A
ENST00000650539.1:n.295G>A
ENST00000330775.9:c.-111G>A	ENSP00000476242.2:n.-111G>A
ENST00000357590.9:c.-111G>A	ENSP00000476176.2:n.-111G>A
ENST00000525039.5:n.313G>A
ENST00000525102.5:n.647G>A
ENST00000525787.1:n.185G>A
ENST00000526626.6:n.85G>A
ENST00000527992.5:n.117G>A
ENST00000530407.5:n.109G>A
ENST00000532085.1:n.1384G>A
ENST00000532888.6:n.85G>A
ENST00000534384.1:n.110G>A
ENST00000538950.5:c.-260G>A	ENSP00000475991.2:n.-260G>A
ENST00000545985.5:c.-111G>A	ENSP00000475241.2:n.-111G>A
NM_001164277.1:c.-111G>A , LRG_187t1:c.-111G>A	NP_001157749.1:n.-111G>A
NM_001164278.1:c.-111G>A	NP_001157750.1:n.-111G>A
NM_001164279.1:c.-260G>A	NP_001157751.1:n.-260G>A
NM_001164280.1:c.-111G>A	NP_001157752.1:n.-111G>A
NM_001467.5:c.-111G>A	NP_001458.1:n.-111G>A
NM_001164278.2:c.-111G>A	NP_001157750.1:n.-111G>A
NM_001164279.2:c.-260G>A	NP_001157751.1:n.-260G>A
NM_001164280.2:c.-111G>A	NP_001157752.1:n.-111G>A
NM_001467.6:c.-111G>A	NP_001458.1:n.-111G>A
NM_001164277.2:c.-111G>A MANE Select	NP_001157749.1:n.-111G>A