Canonical Allele Identifier: CA433165003

Gene: SLC25A38

Linked Data

• MyVariant Identifiers: chr3:g.39436067A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394576A>G , CM000665.2:g.39394576A>G	GRCh38
NC_000003.11:g.39436067A>G , CM000665.1:g.39436067A>G	GRCh37
NC_000003.10:g.39411071A>G	NCBI36
NG_016931.1:g.16253A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000642683.1:c.744A>G	ENSP00000495376.1:p.Lys248=
ENST00000643672.1:c.741A>G	ENSP00000494532.1:p.Lys247=
ENST00000645280.1:c.738A>G	ENSP00000496690.1:p.Lys246=
ENST00000648579.1:c.*89A>G	ENSP00000497638.1:n.*89A>G
ENST00000650617.1:c.792A>G MANE Select	ENSP00000497532.1:p.Lys264=
ENST00000273158.8:c.792A>G	ENSP00000273158.3:p.Lys264=
NM_017875.2:c.792A>G	NP_060345.2:p.Lys264=
XM_006713214.1:c.780A>G	XP_006713277.1:p.Lys260=
XM_011533869.1:c.774A>G	XP_011532171.1:p.Lys258=
XM_011533870.1:c.741A>G	XP_011532172.1:p.Lys247=
XM_011533871.1:c.612A>G	XP_011532173.1:p.Lys204=
NM_001354798.1:c.626-1822A>G	NP_001341727.1:n.626-1822A>G
NM_017875.4:c.792A>G MANE Select	NP_060345.2:p.Lys264=
XM_006713214.2:c.780A>G	XP_006713277.1:p.Lys260=
XM_011533869.2:c.774A>G	XP_011532171.1:p.Lys258=
XM_024453611.1:c.738A>G	XP_024309379.1:p.Lys246=
NM_001354798.2:c.626-1822A>G	NP_001341727.1:n.626-1822A>G