Canonical Allele Identifier: CA2616340730

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119029482-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029482T>A , CM000673.2:g.119029482T>A	GRCh38
NC_000011.9:g.118900192T>A , CM000673.1:g.118900192T>A	GRCh37
NC_000011.8:g.118405402T>A	NCBI36
NG_013331.1:g.6425A>T , LRG_187:g.6425A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.117A>T
ENST00000697846.1:n.117A>T
ENST00000697847.1:n.117A>T
ENST00000697848.1:n.117A>T
ENST00000697849.1:n.361A>T
ENST00000697850.1:n.117A>T
ENST00000697851.1:n.361A>T
ENST00000638186.1:n.191A>T
ENST00000638360.1:n.125A>T
ENST00000638925.1:n.124A>T
ENST00000650539.1:n.293A>T
ENST00000330775.9:c.-113A>T	ENSP00000476242.2:n.-113A>T
ENST00000357590.9:c.-113A>T	ENSP00000476176.2:n.-113A>T
ENST00000525039.5:n.311A>T
ENST00000525102.5:n.645A>T
ENST00000525787.1:n.183A>T
ENST00000526626.6:n.83A>T
ENST00000527992.5:n.115A>T
ENST00000530407.5:n.107A>T
ENST00000532085.1:n.1382A>T
ENST00000532888.6:n.83A>T
ENST00000534384.1:n.108A>T
ENST00000538950.5:c.-262A>T	ENSP00000475991.2:n.-262A>T
ENST00000545985.5:c.-113A>T	ENSP00000475241.2:n.-113A>T
NM_001164277.1:c.-113A>T , LRG_187t1:c.-113A>T	NP_001157749.1:n.-113A>T
NM_001164278.1:c.-113A>T	NP_001157750.1:n.-113A>T
NM_001164279.1:c.-262A>T	NP_001157751.1:n.-262A>T
NM_001164280.1:c.-113A>T	NP_001157752.1:n.-113A>T
NM_001467.5:c.-113A>T	NP_001458.1:n.-113A>T
NM_001164278.2:c.-113A>T	NP_001157750.1:n.-113A>T
NM_001164279.2:c.-262A>T	NP_001157751.1:n.-262A>T
NM_001467.6:c.-113A>T	NP_001458.1:n.-113A>T
NM_001164277.2:c.-113A>T MANE Select	NP_001157749.1:n.-113A>T