Canonical Allele Identifier: CA2616341122

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119029782-TGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029784_119029785del , CM000673.2:g.119029784_119029785del	GRCh38
NC_000011.9:g.118900494_118900495del , CM000673.1:g.118900494_118900495del	GRCh37
NC_000011.8:g.118405704_118405705del	NCBI36
NG_013331.1:g.6123_6124del , LRG_187:g.6123_6124del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.35-220_35-219del
ENST00000697846.1:n.35-220_35-219del
ENST00000697847.1:n.35-220_35-219del
ENST00000697848.1:n.35-220_35-219del
ENST00000697849.1:n.59_60del
ENST00000697850.1:n.35-220_35-219del
ENST00000697851.1:n.59_60del
ENST00000638186.1:n.108+83_108+84del
ENST00000638360.1:n.43-220_43-219del
ENST00000638925.1:n.42-220_42-219del
ENST00000650539.1:n.211-220_211-219del
ENST00000330775.9:c.-195-220_-195-219del	ENSP00000476242.2:n.-195-220_-195-219del
ENST00000357590.9:c.-195-220_-195-219del	ENSP00000476176.2:n.-195-220_-195-219del
ENST00000525039.5:n.229-220_229-219del
ENST00000525102.5:n.563-220_563-219del
ENST00000527992.5:n.33-220_33-219del
ENST00000530407.5:n.25-220_25-219del
ENST00000532085.1:n.1080_1081del
ENST00000534384.1:n.25+132_25+133del
ENST00000538950.5:c.-344-220_-344-219del	ENSP00000475991.2:n.-344-220_-344-219del
ENST00000545985.5:c.-195-220_-195-219del	ENSP00000475241.2:n.-195-220_-195-219del
NM_001164277.1:c.-195-220_-195-219del , LRG_187t1:c.-195-220_-195-219del	NP_001157749.1:n.-195-220_-195-219del
NM_001164278.1:c.-195-220_-195-219del	NP_001157750.1:n.-195-220_-195-219del
NM_001164279.1:c.-344-220_-344-219del	NP_001157751.1:n.-344-220_-344-219del
NM_001467.5:c.-195-220_-195-219del	NP_001458.1:n.-195-220_-195-219del
NM_001164278.2:c.-195-220_-195-219del	NP_001157750.1:n.-195-220_-195-219del
NM_001164279.2:c.-344-220_-344-219del	NP_001157751.1:n.-344-220_-344-219del
NM_001467.6:c.-195-220_-195-219del	NP_001458.1:n.-195-220_-195-219del
NM_001164277.2:c.-195-220_-195-219del MANE Select	NP_001157749.1:n.-195-220_-195-219del