Canonical Allele Identifier: CA2755919900

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394189C>T , CM000665.2:g.39394189C>T	GRCh38
NC_000003.11:g.39435680C>T , CM000665.1:g.39435680C>T	GRCh37
NC_000003.10:g.39410684C>T	NCBI36
NG_016931.1:g.15866C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.578-221C>T	ENSP00000495376.1:n.578-221C>T
ENST00000643672.1:c.575-221C>T	ENSP00000494532.1:n.575-221C>T
ENST00000645280.1:c.572-221C>T	ENSP00000496690.1:n.572-221C>T
ENST00000645630.1:c.446-221C>T	ENSP00000493714.1:n.446-221C>T
ENST00000648579.1:c.722-261C>T	ENSP00000497638.1:n.722-261C>T
ENST00000650617.1:c.626-221C>T MANE Select	ENSP00000497532.1:n.626-221C>T
ENST00000273158.8:c.626-221C>T	ENSP00000273158.3:n.626-221C>T
NM_017875.2:c.626-221C>T	NP_060345.2:n.626-221C>T
XM_006713214.1:c.614-221C>T	XP_006713277.1:n.614-221C>T
XM_011533869.1:c.608-221C>T	XP_011532171.1:n.608-221C>T
XM_011533870.1:c.575-221C>T	XP_011532172.1:n.575-221C>T
XM_011533871.1:c.446-221C>T	XP_011532173.1:n.446-221C>T
NM_001354798.1:c.625+2168C>T	NP_001341727.1:n.625+2168C>T
NM_017875.4:c.626-221C>T MANE Select	NP_060345.2:n.626-221C>T
XM_006713214.2:c.614-221C>T	XP_006713277.1:n.614-221C>T
XM_011533869.2:c.608-221C>T	XP_011532171.1:n.608-221C>T
XM_024453611.1:c.572-221C>T	XP_024309379.1:n.572-221C>T
NM_001354798.2:c.625+2168C>T	NP_001341727.1:n.625+2168C>T