Canonical Allele Identifier: CA2616341132

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119029792-A-ACC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029792_119029793insCC , CM000673.2:g.119029792_119029793insCC	GRCh38
NC_000011.9:g.118900502_118900503insCC , CM000673.1:g.118900502_118900503insCC	GRCh37
NC_000011.8:g.118405712_118405713insCC	NCBI36
NG_013331.1:g.6114_6115insGG , LRG_187:g.6114_6115insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.35-229_35-228insGG
ENST00000697846.1:n.35-229_35-228insGG
ENST00000697847.1:n.35-229_35-228insGG
ENST00000697848.1:n.35-229_35-228insGG
ENST00000697849.1:n.50_51insGG
ENST00000697850.1:n.35-229_35-228insGG
ENST00000697851.1:n.50_51insGG
ENST00000638186.1:n.108+74_108+75insGG
ENST00000638360.1:n.43-229_43-228insGG
ENST00000638925.1:n.42-229_42-228insGG
ENST00000650539.1:n.211-229_211-228insGG
ENST00000330775.9:c.-195-229_-195-228insGG	ENSP00000476242.2:n.-195-229_-195-228insGG
ENST00000357590.9:c.-195-229_-195-228insGG	ENSP00000476176.2:n.-195-229_-195-228insGG
ENST00000525039.5:n.229-229_229-228insGG
ENST00000525102.5:n.563-229_563-228insGG
ENST00000527992.5:n.33-229_33-228insGG
ENST00000530407.5:n.25-229_25-228insGG
ENST00000532085.1:n.1071_1072insGG
ENST00000534384.1:n.25+123_25+124insGG
ENST00000538950.5:c.-344-229_-344-228insGG	ENSP00000475991.2:n.-344-229_-344-228insGG
ENST00000545985.5:c.-195-229_-195-228insGG	ENSP00000475241.2:n.-195-229_-195-228insGG
NM_001164277.1:c.-195-229_-195-228insGG , LRG_187t1:c.-195-229_-195-228insGG	NP_001157749.1:n.-195-229_-195-228insGG
NM_001164278.1:c.-195-229_-195-228insGG	NP_001157750.1:n.-195-229_-195-228insGG
NM_001164279.1:c.-344-229_-344-228insGG	NP_001157751.1:n.-344-229_-344-228insGG
NM_001467.5:c.-195-229_-195-228insGG	NP_001458.1:n.-195-229_-195-228insGG
NM_001164278.2:c.-195-229_-195-228insGG	NP_001157750.1:n.-195-229_-195-228insGG
NM_001164279.2:c.-344-229_-344-228insGG	NP_001157751.1:n.-344-229_-344-228insGG
NM_001467.6:c.-195-229_-195-228insGG	NP_001458.1:n.-195-229_-195-228insGG
NM_001164277.2:c.-195-229_-195-228insGG MANE Select	NP_001157749.1:n.-195-229_-195-228insGG