Canonical Allele Identifier: CA2665163092
Gene: SLC25A38 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39394625_39394626insAAACACC , CM000665.2:g.39394625_39394626insAAACACC GRCh38
NC_000003.11:g.39436116_39436117insAAACACC , CM000665.1:g.39436116_39436117insAAACACC GRCh37
NC_000003.10:g.39411120_39411121insAAACACC NCBI36
NG_016931.1:g.16302_16303insAAACACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000643672.1:c.741+49_741+50insAAACACC ENSP00000494532.1:n.741+49_741+50insAAACACC
ENST00000645280.1:c.738+49_738+50insAAACACC ENSP00000496690.1:n.738+49_738+50insAAACACC
ENST00000648579.1:c.*89+49_*89+50insAAACACC ENSP00000497638.1:n.*89+49_*89+50insAAACACC
ENST00000650617.1:c.792+49_792+50insAAACACC MANE Select ENSP00000497532.1:n.792+49_792+50insAAACACC
ENST00000273158.8:c.792+49_792+50insAAACACC ENSP00000273158.3:n.792+49_792+50insAAACACC
NM_017875.2:c.792+49_792+50insAAACACC NP_060345.2:n.792+49_792+50insAAACACC
XM_006713214.1:c.780+49_780+50insAAACACC XP_006713277.1:n.780+49_780+50insAAACACC
XM_011533869.1:c.774+49_774+50insAAACACC XP_011532171.1:n.774+49_774+50insAAACACC
XM_011533870.1:c.741+49_741+50insAAACACC XP_011532172.1:n.741+49_741+50insAAACACC
XM_011533871.1:c.612+49_612+50insAAACACC XP_011532173.1:n.612+49_612+50insAAACACC
NM_001354798.1:c.626-1773_626-1772insAAACACC NP_001341727.1:n.626-1773_626-1772insAAACACC
NM_017875.4:c.792+49_792+50insAAACACC MANE Select NP_060345.2:n.792+49_792+50insAAACACC
XM_006713214.2:c.780+49_780+50insAAACACC XP_006713277.1:n.780+49_780+50insAAACACC
XM_011533869.2:c.774+49_774+50insAAACACC XP_011532171.1:n.774+49_774+50insAAACACC
XM_024453611.1:c.738+49_738+50insAAACACC XP_024309379.1:n.738+49_738+50insAAACACC
NM_001354798.2:c.626-1773_626-1772insAAACACC NP_001341727.1:n.626-1773_626-1772insAAACACC