Canonical Allele Identifier: CA2327480

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39391882C>T , CM000665.2:g.39391882C>T	GRCh38
NC_000003.11:g.39433373C>T , CM000665.1:g.39433373C>T	GRCh37
NC_000003.10:g.39408377C>T	NCBI36
NG_016931.1:g.13559C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_017875.4:c.486C>T MANE Select	NP_060345.2:p.Tyr162=
ENST00000650617.1:c.486C>T MANE Select	ENSP00000497532.1:p.Tyr162=
NM_001354798.1:c.486C>T	NP_001341727.1:p.Tyr162=
NM_001354798.2:c.486C>T	NP_001341727.1:p.Tyr162=
NM_017875.2:c.486C>T	NP_060345.2:p.Tyr162=
ENST00000273158.8:c.486C>T	ENSP00000273158.3:p.Tyr162=
ENST00000642683.1:c.438C>T	ENSP00000495376.1:p.Tyr146=
ENST00000643672.1:c.435C>T	ENSP00000494532.1:p.Tyr145=
ENST00000645280.1:c.432C>T	ENSP00000496690.1:p.Tyr144=
ENST00000645630.1:c.306C>T	ENSP00000493714.1:p.Tyr102=
ENST00000648579.1:c.486C>T	ENSP00000497638.1:p.Tyr162=
XM_006713214.1:c.474C>T	XP_006713277.1:p.Tyr158=
XM_006713214.2:c.474C>T	XP_006713277.1:p.Tyr158=
XM_011533869.1:c.468C>T	XP_011532171.1:p.Tyr156=
XM_011533869.2:c.468C>T	XP_011532171.1:p.Tyr156=
XM_011533870.1:c.435C>T	XP_011532172.1:p.Tyr145=
XM_011533871.1:c.306C>T	XP_011532173.1:p.Tyr102=
XM_024453611.1:c.432C>T	XP_024309379.1:p.Tyr144=