Canonical Allele Identifier: CA2755920679

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39391425C>T , CM000665.2:g.39391425C>T	GRCh38
NC_000003.11:g.39432916C>T , CM000665.1:g.39432916C>T	GRCh37
NC_000003.10:g.39407920C>T	NCBI36
NG_016931.1:g.13102C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000642683.1:c.229-16C>T	ENSP00000495376.1:n.229-16C>T
ENST00000642978.1:c.259-16C>T	ENSP00000494342.1:n.259-16C>T
ENST00000643672.1:c.226-16C>T	ENSP00000494532.1:n.226-16C>T
ENST00000645280.1:c.223-16C>T	ENSP00000496690.1:n.223-16C>T
ENST00000645630.1:c.277-428C>T	ENSP00000493714.1:n.277-428C>T
ENST00000648579.1:c.277-16C>T	ENSP00000497638.1:n.277-16C>T
ENST00000650617.1:c.277-16C>T MANE Select	ENSP00000497532.1:n.277-16C>T
ENST00000273158.8:c.277-16C>T	ENSP00000273158.3:n.277-16C>T
ENST00000431510.1:c.265-16C>T	ENSP00000394244.1:n.265-16C>T
NM_017875.2:c.277-16C>T	NP_060345.2:n.277-16C>T
XM_006713214.1:c.265-16C>T	XP_006713277.1:n.265-16C>T
XM_011533869.1:c.259-16C>T	XP_011532171.1:n.259-16C>T
XM_011533870.1:c.226-16C>T	XP_011532172.1:n.226-16C>T
XM_011533871.1:c.277-428C>T	XP_011532173.1:n.277-428C>T
NM_001354798.1:c.277-16C>T	NP_001341727.1:n.277-16C>T
NM_017875.4:c.277-16C>T MANE Select	NP_060345.2:n.277-16C>T
XM_006713214.2:c.265-16C>T	XP_006713277.1:n.265-16C>T
XM_011533869.2:c.259-16C>T	XP_011532171.1:n.259-16C>T
XM_024453611.1:c.223-16C>T	XP_024309379.1:n.223-16C>T
NM_001354798.2:c.277-16C>T	NP_001341727.1:n.277-16C>T