Canonical Allele Identifier: CA2616341584

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119030434-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119030434C>T , CM000673.2:g.119030434C>T	GRCh38
NC_000011.9:g.118901144C>T , CM000673.1:g.118901144C>T	GRCh37
NC_000011.8:g.118406354C>T	NCBI36
NG_013331.1:g.5473G>A , LRG_187:g.5473G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.34+415G>A
ENST00000697846.1:n.34+415G>A
ENST00000697847.1:n.34+415G>A
ENST00000697848.1:n.34+415G>A
ENST00000697850.1:n.34+415G>A
ENST00000638360.1:n.42+415G>A
ENST00000638925.1:n.41+415G>A
ENST00000330775.9:c.-196+415G>A	ENSP00000476242.2:n.-196+415G>A
ENST00000357590.9:c.-196+114G>A	ENSP00000476176.2:n.-196+114G>A
ENST00000525039.5:n.228+114G>A
ENST00000525102.5:n.360G>A
ENST00000527992.5:n.32+415G>A
ENST00000530407.5:n.24+415G>A
ENST00000532085.1:n.430G>A
ENST00000538950.5:c.-345+415G>A	ENSP00000475991.2:n.-345+415G>A
ENST00000545985.5:c.-398G>A	ENSP00000475241.2:n.-398G>A
NM_001164277.1:c.-398G>A , LRG_187t1:c.-398G>A	NP_001157749.1:n.-398G>A
NM_001164278.1:c.-196+114G>A	NP_001157750.1:n.-196+114G>A
NM_001164279.1:c.-345+415G>A	NP_001157751.1:n.-345+415G>A
NM_001467.5:c.-196+415G>A	NP_001458.1:n.-196+415G>A
NM_001164278.2:c.-196+114G>A	NP_001157750.1:n.-196+114G>A
NM_001164279.2:c.-345+415G>A	NP_001157751.1:n.-345+415G>A
NM_001467.6:c.-196+415G>A	NP_001458.1:n.-196+415G>A
NM_001164277.2:c.-398G>A MANE Select	NP_001157749.1:n.-398G>A