Canonical Allele Identifier: CA2003775933

Gene: SLC37A4

Linked Data

• dbSNP Id: rs1943695079

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029858_119029860del , CM000673.2:g.119029858_119029860del	GRCh38
NC_000011.9:g.118900568_118900570del , CM000673.1:g.118900568_118900570del	GRCh37
NC_000011.8:g.118405778_118405780del	NCBI36
NG_013331.1:g.6050_6052del , LRG_187:g.6050_6052del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.35-293_35-291del
ENST00000697846.1:n.35-293_35-291del
ENST00000697847.1:n.35-293_35-291del
ENST00000697848.1:n.35-293_35-291del
ENST00000697850.1:n.35-293_35-291del
ENST00000638186.1:n.108+10_108+12del
ENST00000638360.1:n.43-293_43-291del
ENST00000638925.1:n.42-293_42-291del
ENST00000650539.1:n.211-293_211-291del
ENST00000330775.9:c.-195-293_-195-291del	ENSP00000476242.2:n.-195-293_-195-291del
ENST00000357590.9:c.-195-293_-195-291del	ENSP00000476176.2:n.-195-293_-195-291del
ENST00000525039.5:n.229-293_229-291del
ENST00000525102.5:n.563-293_563-291del
ENST00000527992.5:n.33-293_33-291del
ENST00000530407.5:n.25-293_25-291del
ENST00000532085.1:n.1007_1009del
ENST00000534384.1:n.25+59_25+61del
ENST00000538950.5:c.-344-293_-344-291del	ENSP00000475991.2:n.-344-293_-344-291del
ENST00000545985.5:c.-195-293_-195-291del	ENSP00000475241.2:n.-195-293_-195-291del
NM_001164277.1:c.-195-293_-195-291del , LRG_187t1:c.-195-293_-195-291del	NP_001157749.1:n.-195-293_-195-291del
NM_001164278.1:c.-195-293_-195-291del	NP_001157750.1:n.-195-293_-195-291del
NM_001164279.1:c.-344-293_-344-291del	NP_001157751.1:n.-344-293_-344-291del
NM_001467.5:c.-195-293_-195-291del	NP_001458.1:n.-195-293_-195-291del
NM_001164278.2:c.-195-293_-195-291del	NP_001157750.1:n.-195-293_-195-291del
NM_001164279.2:c.-344-293_-344-291del	NP_001157751.1:n.-344-293_-344-291del
NM_001467.6:c.-195-293_-195-291del	NP_001458.1:n.-195-293_-195-291del
NM_001164277.2:c.-195-293_-195-291del MANE Select	NP_001157749.1:n.-195-293_-195-291del