Canonical Allele Identifier: CA433164652

Gene: SLC25A38

Linked Data

• MyVariant Identifiers: chr3:g.39435986T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394495T>C , CM000665.2:g.39394495T>C	GRCh38
NC_000003.11:g.39435986T>C , CM000665.1:g.39435986T>C	GRCh37
NC_000003.10:g.39410990T>C	NCBI36
NG_016931.1:g.16172T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.663T>C	ENSP00000495376.1:p.Pro221=
ENST00000643672.1:c.660T>C	ENSP00000494532.1:p.Pro220=
ENST00000645280.1:c.657T>C	ENSP00000496690.1:p.Pro219=
ENST00000648579.1:c.*8T>C	ENSP00000497638.1:n.*8T>C
ENST00000650617.1:c.711T>C MANE Select	ENSP00000497532.1:p.Pro237=
ENST00000273158.8:c.711T>C	ENSP00000273158.3:p.Pro237=
NM_017875.2:c.711T>C	NP_060345.2:p.Pro237=
XM_006713214.1:c.699T>C	XP_006713277.1:p.Pro233=
XM_011533869.1:c.693T>C	XP_011532171.1:p.Pro231=
XM_011533870.1:c.660T>C	XP_011532172.1:p.Pro220=
XM_011533871.1:c.531T>C	XP_011532173.1:p.Pro177=
NM_001354798.1:c.626-1903T>C	NP_001341727.1:n.626-1903T>C
NM_017875.4:c.711T>C MANE Select	NP_060345.2:p.Pro237=
XM_006713214.2:c.699T>C	XP_006713277.1:p.Pro233=
XM_011533869.2:c.693T>C	XP_011532171.1:p.Pro231=
XM_024453611.1:c.657T>C	XP_024309379.1:p.Pro219=
NM_001354798.2:c.626-1903T>C	NP_001341727.1:n.626-1903T>C