Canonical Allele Identifier: CA352199083

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39389600C>T , CM000665.2:g.39389600C>T	GRCh38
NC_000003.11:g.39431091C>T , CM000665.1:g.39431091C>T	GRCh37
NC_000003.10:g.39406095C>T	NCBI36
NG_016931.1:g.11277C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642442.1:n.236C>T
ENST00000642683.1:c.175C>T	ENSP00000495376.1:p.Gln59Ter
ENST00000642978.1:c.157C>T	ENSP00000494342.1:p.Gln53Ter
ENST00000643672.1:c.124C>T	ENSP00000494532.1:p.Gln42Ter
ENST00000645280.1:c.121C>T	ENSP00000496690.1:p.Gln41Ter
ENST00000645630.1:c.175C>T	ENSP00000493714.1:p.Gln59Ter
ENST00000648579.1:c.175C>T	ENSP00000497638.1:p.Gln59Ter
ENST00000650617.1:c.175C>T MANE Select	ENSP00000497532.1:p.Gln59Ter
ENST00000273158.8:c.175C>T	ENSP00000273158.3:p.Gln59Ter
ENST00000431510.1:c.163C>T	ENSP00000394244.1:p.Gln55Ter
NM_017875.2:c.175C>T	NP_060345.2:p.Gln59Ter
XM_006713214.1:c.163C>T	XP_006713277.1:p.Gln55Ter
XM_011533869.1:c.157C>T	XP_011532171.1:p.Gln53Ter
XM_011533870.1:c.124C>T	XP_011532172.1:p.Gln42Ter
XM_011533871.1:c.175C>T	XP_011532173.1:p.Gln59Ter
NM_001354798.1:c.175C>T	NP_001341727.1:p.Gln59Ter
NM_017875.4:c.175C>T MANE Select	NP_060345.2:p.Gln59Ter
XM_006713214.2:c.163C>T	XP_006713277.1:p.Gln55Ter
XM_011533869.2:c.157C>T	XP_011532171.1:p.Gln53Ter
XM_024453611.1:c.121C>T	XP_024309379.1:p.Gln41Ter
NM_001354798.2:c.175C>T	NP_001341727.1:p.Gln59Ter