Canonical Allele Identifier: CA2755919946

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394578_39394581del , CM000665.2:g.39394578_39394581del	GRCh38
NC_000003.11:g.39436069_39436072del , CM000665.1:g.39436069_39436072del	GRCh37
NC_000003.10:g.39411073_39411076del	NCBI36
NG_016931.1:g.16255_16258del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643672.1:c.741+2_741+5del
ENST00000645280.1:c.738+2_738+5del
ENST00000648579.1:c.*89+2_*89+5del
ENST00000650617.1:c.792+2_792+5del
ENST00000273158.8:c.792+2_792+5del
NM_017875.2:c.792+2_792+5del
XM_006713214.1:c.780+2_780+5del
XM_011533869.1:c.774+2_774+5del
XM_011533870.1:c.741+2_741+5del
XM_011533871.1:c.612+2_612+5del
NM_001354798.1:c.626-1820_626-1817del	NP_001341727.1:n.626-1820_626-1817del
NM_017875.4:c.792+2_792+5del
XM_006713214.2:c.780+2_780+5del
XM_011533869.2:c.774+2_774+5del
XM_024453611.1:c.738+2_738+5del
NM_001354798.2:c.626-1820_626-1817del	NP_001341727.1:n.626-1820_626-1817del