Canonical Allele Identifier: CA2665163097

Gene: SLC25A38

Linked Data

• gnomAD v4: 3-39394630-G-GTA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394630_39394631insTA , CM000665.2:g.39394630_39394631insTA	GRCh38
NC_000003.11:g.39436121_39436122insTA , CM000665.1:g.39436121_39436122insTA	GRCh37
NC_000003.10:g.39411125_39411126insTA	NCBI36
NG_016931.1:g.16307_16308insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643672.1:c.741+54_741+55insTA	ENSP00000494532.1:n.741+54_741+55insTA
ENST00000645280.1:c.738+54_738+55insTA	ENSP00000496690.1:n.738+54_738+55insTA
ENST00000648579.1:c.*89+54_*89+55insTA	ENSP00000497638.1:n.*89+54_*89+55insTA
ENST00000650617.1:c.792+54_792+55insTA MANE Select	ENSP00000497532.1:n.792+54_792+55insTA
ENST00000273158.8:c.792+54_792+55insTA	ENSP00000273158.3:n.792+54_792+55insTA
NM_017875.2:c.792+54_792+55insTA	NP_060345.2:n.792+54_792+55insTA
XM_006713214.1:c.780+54_780+55insTA	XP_006713277.1:n.780+54_780+55insTA
XM_011533869.1:c.774+54_774+55insTA	XP_011532171.1:n.774+54_774+55insTA
XM_011533870.1:c.741+54_741+55insTA	XP_011532172.1:n.741+54_741+55insTA
XM_011533871.1:c.612+54_612+55insTA	XP_011532173.1:n.612+54_612+55insTA
NM_001354798.1:c.626-1768_626-1767insTA	NP_001341727.1:n.626-1768_626-1767insTA
NM_017875.4:c.792+54_792+55insTA MANE Select	NP_060345.2:n.792+54_792+55insTA
XM_006713214.2:c.780+54_780+55insTA	XP_006713277.1:n.780+54_780+55insTA
XM_011533869.2:c.774+54_774+55insTA	XP_011532171.1:n.774+54_774+55insTA
XM_024453611.1:c.738+54_738+55insTA	XP_024309379.1:n.738+54_738+55insTA
NM_001354798.2:c.626-1768_626-1767insTA	NP_001341727.1:n.626-1768_626-1767insTA