Canonical Allele Identifier: CA2517282800

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39397059C>G , CM000665.2:g.39397059C>G	GRCh38
NC_000003.11:g.39438550C>G , CM000665.1:g.39438550C>G	GRCh37
NC_000003.10:g.39413554C>G	NCBI36
NG_016931.1:g.18736C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648579.1:c.*751C>G	ENSP00000497638.1:n.*751C>G
ENST00000650617.1:c.*539C>G MANE Select	ENSP00000497532.1:n.*539C>G
ENST00000273158.8:c.*539C>G	ENSP00000273158.3:n.*539C>G
NM_017875.2:c.*539C>G	NP_060345.2:n.*539C>G
XM_006713214.1:c.*539C>G	XP_006713277.1:n.*539C>G
XM_011533869.1:c.*539C>G	XP_011532171.1:n.*539C>G
XM_011533870.1:c.*539C>G	XP_011532172.1:n.*539C>G
XM_011533871.1:c.*539C>G	XP_011532173.1:n.*539C>G
NM_001354798.1:c.*573C>G	NP_001341727.1:n.*573C>G
NM_017875.4:c.*539C>G MANE Select	NP_060345.2:n.*539C>G
XM_006713214.2:c.*539C>G	XP_006713277.1:n.*539C>G
XM_011533869.2:c.*539C>G	XP_011532171.1:n.*539C>G
XM_024453611.1:c.*539C>G	XP_024309379.1:n.*539C>G
NM_001354798.2:c.*573C>G	NP_001341727.1:n.*573C>G