Canonical Allele Identifier: CA352205676

Gene: SLC25A38

Linked Data

• MyVariant Identifiers: chr3:g.39436045A>C (hg19) ; chr3:g.39394554A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394554A>C , CM000665.2:g.39394554A>C	GRCh38
NC_000003.11:g.39436045A>C , CM000665.1:g.39436045A>C	GRCh37
NC_000003.10:g.39411049A>C	NCBI36
NG_016931.1:g.16231A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.722A>C	ENSP00000495376.1:p.Gln241Pro
ENST00000643672.1:c.719A>C	ENSP00000494532.1:p.Gln240Pro
ENST00000645280.1:c.716A>C	ENSP00000496690.1:p.Gln239Pro
ENST00000648579.1:c.*67A>C	ENSP00000497638.1:n.*67A>C
ENST00000650617.1:c.770A>C MANE Select	ENSP00000497532.1:p.Gln257Pro
ENST00000273158.8:c.770A>C	ENSP00000273158.3:p.Gln257Pro
NM_017875.2:c.770A>C	NP_060345.2:p.Gln257Pro
XM_006713214.1:c.758A>C	XP_006713277.1:p.Gln253Pro
XM_011533869.1:c.752A>C	XP_011532171.1:p.Gln251Pro
XM_011533870.1:c.719A>C	XP_011532172.1:p.Gln240Pro
XM_011533871.1:c.590A>C	XP_011532173.1:p.Gln197Pro
NM_001354798.1:c.626-1844A>C	NP_001341727.1:n.626-1844A>C
NM_017875.4:c.770A>C MANE Select	NP_060345.2:p.Gln257Pro
XM_006713214.2:c.758A>C	XP_006713277.1:p.Gln253Pro
XM_011533869.2:c.752A>C	XP_011532171.1:p.Gln251Pro
XM_024453611.1:c.716A>C	XP_024309379.1:p.Gln239Pro
NM_001354798.2:c.626-1844A>C	NP_001341727.1:n.626-1844A>C