Canonical Allele Identifier: CA2616340675

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119029414-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029416dup , CM000673.2:g.119029416dup	GRCh38
NC_000011.9:g.118900126dup , CM000673.1:g.118900126dup	GRCh37
NC_000011.8:g.118405336dup	NCBI36
NG_013331.1:g.6492dup , LRG_187:g.6492dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.184dup
ENST00000697846.1:n.184dup
ENST00000697847.1:n.184dup
ENST00000697848.1:n.184dup
ENST00000697849.1:n.428dup
ENST00000697850.1:n.184dup
ENST00000697851.1:n.428dup
ENST00000638186.1:n.258dup
ENST00000638360.1:n.192dup
ENST00000638925.1:n.191dup
ENST00000650539.1:n.360dup
ENST00000330775.9:c.-46dup	ENSP00000476242.2:n.-46dup
ENST00000357590.9:c.-46dup	ENSP00000476176.2:n.-46dup
ENST00000525039.5:n.378dup
ENST00000525102.5:n.712dup
ENST00000525787.1:n.250dup
ENST00000526626.6:n.150dup
ENST00000527992.5:n.182dup
ENST00000530407.5:n.174dup
ENST00000532085.1:n.1449dup
ENST00000532888.6:n.150dup
ENST00000534384.1:n.175dup
ENST00000538950.5:c.-195dup	ENSP00000475991.2:n.-195dup
ENST00000545985.5:c.-46dup	ENSP00000475241.2:n.-46dup
NM_001164277.1:c.-46dup , LRG_187t1:c.-46dup	NP_001157749.1:n.-46dup
NM_001164278.1:c.-46dup	NP_001157750.1:n.-46dup
NM_001164279.1:c.-195dup	NP_001157751.1:n.-195dup
NM_001164280.1:c.-46dup	NP_001157752.1:n.-46dup
NM_001467.5:c.-46dup	NP_001458.1:n.-46dup
NM_001164278.2:c.-46dup	NP_001157750.1:n.-46dup
NM_001164279.2:c.-195dup	NP_001157751.1:n.-195dup
NM_001164280.2:c.-46dup	NP_001157752.1:n.-46dup
NM_001467.6:c.-46dup	NP_001458.1:n.-46dup
NM_001164277.2:c.-46dup MANE Select	NP_001157749.1:n.-46dup