Canonical Allele Identifier: CA2665162914

Gene: SLC25A38

Linked Data

• gnomAD v4: 3-39394413-AGGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394416_39394418del , CM000665.2:g.39394416_39394418del	GRCh38
NC_000003.11:g.39435907_39435909del , CM000665.1:g.39435907_39435909del	GRCh37
NC_000003.10:g.39410911_39410913del	NCBI36
NG_016931.1:g.16093_16095del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.584_586del	ENSP00000495376.1:p.Val195del
ENST00000643672.1:c.581_583del	ENSP00000494532.1:p.Val194del
ENST00000645280.1:c.578_580del	ENSP00000496690.1:p.Val193del
ENST00000645630.1:c.452_454del	ENSP00000493714.1:p.Val151del
ENST00000648579.1:c.722-34_722-32del	ENSP00000497638.1:n.722-34_722-32del
ENST00000650617.1:c.632_634del MANE Select	ENSP00000497532.1:p.Val211del
ENST00000273158.8:c.632_634del	ENSP00000273158.3:p.Val211del
NM_017875.2:c.632_634del	NP_060345.2:p.Val211del
XM_006713214.1:c.620_622del	XP_006713277.1:p.Val207del
XM_011533869.1:c.614_616del	XP_011532171.1:p.Val205del
XM_011533870.1:c.581_583del	XP_011532172.1:p.Val194del
XM_011533871.1:c.452_454del	XP_011532173.1:p.Val151del
NM_001354798.1:c.626-1982_626-1980del	NP_001341727.1:n.626-1982_626-1980del
NM_017875.4:c.632_634del MANE Select	NP_060345.2:p.Val211del
XM_006713214.2:c.620_622del	XP_006713277.1:p.Val207del
XM_011533869.2:c.614_616del	XP_011532171.1:p.Val205del
XM_024453611.1:c.578_580del	XP_024309379.1:p.Val193del
NM_001354798.2:c.626-1982_626-1980del	NP_001341727.1:n.626-1982_626-1980del