Canonical Allele Identifier: CA2003775944

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029868_119029869delinsAG , CM000673.2:g.119029868_119029869delinsAG	GRCh38
NC_000011.9:g.118900578_118900579delinsAG , CM000673.1:g.118900578_118900579delinsAG	GRCh37
NC_000011.8:g.118405788_118405789delinsAG	NCBI36
NG_013331.1:g.6038_6039delinsCT , LRG_187:g.6038_6039delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.35-305_35-304delinsCT
ENST00000697846.1:n.35-305_35-304delinsCT
ENST00000697847.1:n.35-305_35-304delinsCT
ENST00000697848.1:n.35-305_35-304delinsCT
ENST00000697850.1:n.35-305_35-304delinsCT
ENST00000638186.1:n.106_107delinsCT
ENST00000638360.1:n.43-305_43-304delinsCT
ENST00000638925.1:n.42-305_42-304delinsCT
ENST00000650539.1:n.210+301_210+302delinsCT
ENST00000330775.9:c.-195-305_-195-304delinsCT	ENSP00000476242.2:n.-195-305_-195-304delinsCT
ENST00000357590.9:c.-195-305_-195-304delinsCT	ENSP00000476176.2:n.-195-305_-195-304delinsCT
ENST00000525039.5:n.229-305_229-304delinsCT
ENST00000525102.5:n.563-305_563-304delinsCT
ENST00000527992.5:n.33-305_33-304delinsCT
ENST00000530407.5:n.25-305_25-304delinsCT
ENST00000532085.1:n.995_996delinsCT
ENST00000534384.1:n.25+47_25+48delinsCT
ENST00000538950.5:c.-344-305_-344-304delinsCT	ENSP00000475991.2:n.-344-305_-344-304delinsCT
ENST00000545985.5:c.-195-305_-195-304delinsCT	ENSP00000475241.2:n.-195-305_-195-304delinsCT
NM_001164277.1:c.-195-305_-195-304delinsCT , LRG_187t1:c.-195-305_-195-304delinsCT	NP_001157749.1:n.-195-305_-195-304delinsCT
NM_001164278.1:c.-195-305_-195-304delinsCT	NP_001157750.1:n.-195-305_-195-304delinsCT
NM_001164279.1:c.-344-305_-344-304delinsCT	NP_001157751.1:n.-344-305_-344-304delinsCT
NM_001467.5:c.-195-305_-195-304delinsCT	NP_001458.1:n.-195-305_-195-304delinsCT
NM_001164278.2:c.-195-305_-195-304delinsCT	NP_001157750.1:n.-195-305_-195-304delinsCT
NM_001164279.2:c.-344-305_-344-304delinsCT	NP_001157751.1:n.-344-305_-344-304delinsCT
NM_001467.6:c.-195-305_-195-304delinsCT	NP_001458.1:n.-195-305_-195-304delinsCT
NM_001164277.2:c.-195-305_-195-304delinsCT MANE Select	NP_001157749.1:n.-195-305_-195-304delinsCT