Canonical Allele Identifier: CA2616341174

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119029835-CTCAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029843_119029846del , CM000673.2:g.119029843_119029846del	GRCh38
NC_000011.9:g.118900553_118900556del , CM000673.1:g.118900553_118900556del	GRCh37
NC_000011.8:g.118405763_118405766del	NCBI36
NG_013331.1:g.6068_6071del , LRG_187:g.6068_6071del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.35-275_35-272del
ENST00000697846.1:n.35-275_35-272del
ENST00000697847.1:n.35-275_35-272del
ENST00000697848.1:n.35-275_35-272del
ENST00000697850.1:n.35-275_35-272del
ENST00000638186.1:n.108+28_108+31del
ENST00000638360.1:n.43-275_43-272del
ENST00000638925.1:n.42-275_42-272del
ENST00000650539.1:n.211-275_211-272del
ENST00000330775.9:c.-195-275_-195-272del	ENSP00000476242.2:n.-195-275_-195-272del
ENST00000357590.9:c.-195-275_-195-272del	ENSP00000476176.2:n.-195-275_-195-272del
ENST00000525039.5:n.229-275_229-272del
ENST00000525102.5:n.563-275_563-272del
ENST00000527992.5:n.33-275_33-272del
ENST00000530407.5:n.25-275_25-272del
ENST00000532085.1:n.1025_1028del
ENST00000534384.1:n.25+77_25+80del
ENST00000538950.5:c.-344-275_-344-272del	ENSP00000475991.2:n.-344-275_-344-272del
ENST00000545985.5:c.-195-275_-195-272del	ENSP00000475241.2:n.-195-275_-195-272del
NM_001164277.1:c.-195-275_-195-272del , LRG_187t1:c.-195-275_-195-272del	NP_001157749.1:n.-195-275_-195-272del
NM_001164278.1:c.-195-275_-195-272del	NP_001157750.1:n.-195-275_-195-272del
NM_001164279.1:c.-344-275_-344-272del	NP_001157751.1:n.-344-275_-344-272del
NM_001467.5:c.-195-275_-195-272del	NP_001458.1:n.-195-275_-195-272del
NM_001164278.2:c.-195-275_-195-272del	NP_001157750.1:n.-195-275_-195-272del
NM_001164279.2:c.-344-275_-344-272del	NP_001157751.1:n.-344-275_-344-272del
NM_001467.6:c.-195-275_-195-272del	NP_001458.1:n.-195-275_-195-272del
NM_001164277.2:c.-195-275_-195-272del MANE Select	NP_001157749.1:n.-195-275_-195-272del