Canonical Allele Identifier: CA229601776

Gene: SLC37A4

Linked Data

• dbSNP Id: rs930159364
• gnomAD v2: 11-118900632-C-T
• gnomAD v3: 11-119029922-C-T
• gnomAD v4: 11-119029922-C-T
• MyVariant Identifiers: chr11:g.118900632C>T (hg19) ; chr11:g.119029922C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029922C>T , CM000673.2:g.119029922C>T	GRCh38
NC_000011.9:g.118900632C>T , CM000673.1:g.118900632C>T	GRCh37
NC_000011.8:g.118405842C>T	NCBI36
NG_013331.1:g.5985G>A , LRG_187:g.5985G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.35-358G>A
ENST00000697846.1:n.35-358G>A
ENST00000697847.1:n.35-358G>A
ENST00000697848.1:n.35-358G>A
ENST00000697850.1:n.35-358G>A
ENST00000638186.1:n.53G>A
ENST00000638360.1:n.43-358G>A
ENST00000638925.1:n.42-358G>A
ENST00000650539.1:n.210+248G>A
ENST00000330775.9:c.-195-358G>A	ENSP00000476242.2:n.-195-358G>A
ENST00000357590.9:c.-195-358G>A	ENSP00000476176.2:n.-195-358G>A
ENST00000525039.5:n.229-358G>A
ENST00000525102.5:n.562+310G>A
ENST00000527992.5:n.33-358G>A
ENST00000530407.5:n.25-358G>A
ENST00000532085.1:n.942G>A
ENST00000534384.1:n.19G>A
ENST00000538950.5:c.-344-358G>A	ENSP00000475991.2:n.-344-358G>A
ENST00000545985.5:c.-196+310G>A	ENSP00000475241.2:n.-196+310G>A
NM_001164277.1:c.-196+310G>A , LRG_187t1:c.-196+310G>A	NP_001157749.1:n.-196+310G>A
NM_001164278.1:c.-195-358G>A	NP_001157750.1:n.-195-358G>A
NM_001164279.1:c.-344-358G>A	NP_001157751.1:n.-344-358G>A
NM_001467.5:c.-195-358G>A	NP_001458.1:n.-195-358G>A
NM_001164278.2:c.-195-358G>A	NP_001157750.1:n.-195-358G>A
NM_001164279.2:c.-344-358G>A	NP_001157751.1:n.-344-358G>A
NM_001467.6:c.-195-358G>A	NP_001458.1:n.-195-358G>A
NM_001164277.2:c.-196+310G>A MANE Select	NP_001157749.1:n.-196+310G>A