Canonical Allele Identifier: CA2616340738

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119029487-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029487C>A , CM000673.2:g.119029487C>A	GRCh38
NC_000011.9:g.118900197C>A , CM000673.1:g.118900197C>A	GRCh37
NC_000011.8:g.118405407C>A	NCBI36
NG_013331.1:g.6420G>T , LRG_187:g.6420G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.112G>T
ENST00000697846.1:n.112G>T
ENST00000697847.1:n.112G>T
ENST00000697848.1:n.112G>T
ENST00000697849.1:n.356G>T
ENST00000697850.1:n.112G>T
ENST00000697851.1:n.356G>T
ENST00000638186.1:n.186G>T
ENST00000638360.1:n.120G>T
ENST00000638925.1:n.119G>T
ENST00000650539.1:n.288G>T
ENST00000330775.9:c.-118G>T	ENSP00000476242.2:n.-118G>T
ENST00000357590.9:c.-118G>T	ENSP00000476176.2:n.-118G>T
ENST00000525039.5:n.306G>T
ENST00000525102.5:n.640G>T
ENST00000525787.1:n.178G>T
ENST00000526626.6:n.78G>T
ENST00000527992.5:n.110G>T
ENST00000530407.5:n.102G>T
ENST00000532085.1:n.1377G>T
ENST00000532888.6:n.78G>T
ENST00000534384.1:n.103G>T
ENST00000538950.5:c.-267G>T	ENSP00000475991.2:n.-267G>T
ENST00000545985.5:c.-118G>T	ENSP00000475241.2:n.-118G>T
NM_001164277.1:c.-118G>T , LRG_187t1:c.-118G>T	NP_001157749.1:n.-118G>T
NM_001164278.1:c.-118G>T	NP_001157750.1:n.-118G>T
NM_001164279.1:c.-267G>T	NP_001157751.1:n.-267G>T
NM_001164280.1:c.-118G>T	NP_001157752.1:n.-118G>T
NM_001467.5:c.-118G>T	NP_001458.1:n.-118G>T
NM_001164278.2:c.-118G>T	NP_001157750.1:n.-118G>T
NM_001164279.2:c.-267G>T	NP_001157751.1:n.-267G>T
NM_001467.6:c.-118G>T	NP_001458.1:n.-118G>T
NM_001164277.2:c.-118G>T MANE Select	NP_001157749.1:n.-118G>T