Canonical Allele Identifier: CA229601313

Gene: SLC37A4

Linked Data

• dbSNP Id: rs782232636
• gnomAD v2: 11-118900120-T-A
• gnomAD v4: 11-119029410-T-A
• MyVariant Identifiers: chr11:g.118900120T>A (hg19) ; chr11:g.119029410T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029410T>A , CM000673.2:g.119029410T>A	GRCh38
NC_000011.9:g.118900120T>A , CM000673.1:g.118900120T>A	GRCh37
NC_000011.8:g.118405330T>A	NCBI36
NG_013331.1:g.6497A>T , LRG_187:g.6497A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.189A>T
ENST00000697846.1:n.189A>T
ENST00000697847.1:n.189A>T
ENST00000697848.1:n.189A>T
ENST00000697849.1:n.433A>T
ENST00000697850.1:n.189A>T
ENST00000697851.1:n.433A>T
ENST00000638186.1:n.263A>T
ENST00000638360.1:n.197A>T
ENST00000638925.1:n.196A>T
ENST00000650539.1:n.365A>T
ENST00000330775.9:c.-41A>T	ENSP00000476242.2:n.-41A>T
ENST00000357590.9:c.-41A>T	ENSP00000476176.2:n.-41A>T
ENST00000525039.5:n.383A>T
ENST00000525102.5:n.717A>T
ENST00000525787.1:n.255A>T
ENST00000526626.6:n.155A>T
ENST00000527992.5:n.187A>T
ENST00000530407.5:n.179A>T
ENST00000532085.1:n.1454A>T
ENST00000532888.6:n.155A>T
ENST00000534384.1:n.180A>T
ENST00000538950.5:c.-190A>T	ENSP00000475991.2:n.-190A>T
ENST00000545985.5:c.-41A>T	ENSP00000475241.2:n.-41A>T
NM_001164277.1:c.-41A>T , LRG_187t1:c.-41A>T	NP_001157749.1:n.-41A>T
NM_001164278.1:c.-41A>T	NP_001157750.1:n.-41A>T
NM_001164279.1:c.-190A>T	NP_001157751.1:n.-190A>T
NM_001164280.1:c.-41A>T	NP_001157752.1:n.-41A>T
NM_001467.5:c.-41A>T	NP_001458.1:n.-41A>T
NM_001164278.2:c.-41A>T	NP_001157750.1:n.-41A>T
NM_001164279.2:c.-190A>T	NP_001157751.1:n.-190A>T
NM_001164280.2:c.-41A>T	NP_001157752.1:n.-41A>T
NM_001467.6:c.-41A>T	NP_001458.1:n.-41A>T
NM_001164277.2:c.-41A>T MANE Select	NP_001157749.1:n.-41A>T