Canonical Allele Identifier: CA2616340761

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119029504-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029507del , CM000673.2:g.119029507del	GRCh38
NC_000011.9:g.118900217del , CM000673.1:g.118900217del	GRCh37
NC_000011.8:g.118405427del	NCBI36
NG_013331.1:g.6402del , LRG_187:g.6402del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.94del
ENST00000697846.1:n.94del
ENST00000697847.1:n.94del
ENST00000697848.1:n.94del
ENST00000697849.1:n.338del
ENST00000697850.1:n.94del
ENST00000697851.1:n.338del
ENST00000638186.1:n.168del
ENST00000638360.1:n.102del
ENST00000638925.1:n.101del
ENST00000650539.1:n.270del
ENST00000330775.9:c.-136del	ENSP00000476242.2:n.-136del
ENST00000357590.9:c.-136del	ENSP00000476176.2:n.-136del
ENST00000525039.5:n.288del
ENST00000525102.5:n.622del
ENST00000525787.1:n.160del
ENST00000526626.6:n.60del
ENST00000527992.5:n.92del
ENST00000530407.5:n.84del
ENST00000532085.1:n.1359del
ENST00000532888.6:n.60del
ENST00000534384.1:n.85del
ENST00000538950.5:c.-285del	ENSP00000475991.2:n.-285del
ENST00000545985.5:c.-136del	ENSP00000475241.2:n.-136del
NM_001164277.1:c.-136del , LRG_187t1:c.-136del	NP_001157749.1:n.-136del
NM_001164278.1:c.-136del	NP_001157750.1:n.-136del
NM_001164279.1:c.-285del	NP_001157751.1:n.-285del
NM_001164280.1:c.-136del	NP_001157752.1:n.-136del
NM_001467.5:c.-136del	NP_001458.1:n.-136del
NM_001164278.2:c.-136del	NP_001157750.1:n.-136del
NM_001164279.2:c.-285del	NP_001157751.1:n.-285del
NM_001467.6:c.-136del	NP_001458.1:n.-136del
NM_001164277.2:c.-136del MANE Select	NP_001157749.1:n.-136del