Canonical Allele Identifier: CA352205827

Gene: SLC25A38

Linked Data

• MyVariant Identifiers: chr3:g.39436063T>C (hg19) ; chr3:g.39394572T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394572T>C , CM000665.2:g.39394572T>C	GRCh38
NC_000003.11:g.39436063T>C , CM000665.1:g.39436063T>C	GRCh37
NC_000003.10:g.39411067T>C	NCBI36
NG_016931.1:g.16249T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.740T>C	ENSP00000495376.1:p.Phe247Ser
ENST00000643672.1:c.737T>C	ENSP00000494532.1:p.Phe246Ser
ENST00000645280.1:c.734T>C	ENSP00000496690.1:p.Phe245Ser
ENST00000648579.1:c.*85T>C	ENSP00000497638.1:n.*85T>C
ENST00000650617.1:c.788T>C MANE Select	ENSP00000497532.1:p.Phe263Ser
ENST00000273158.8:c.788T>C	ENSP00000273158.3:p.Phe263Ser
NM_017875.2:c.788T>C	NP_060345.2:p.Phe263Ser
XM_006713214.1:c.776T>C	XP_006713277.1:p.Phe259Ser
XM_011533869.1:c.770T>C	XP_011532171.1:p.Phe257Ser
XM_011533870.1:c.737T>C	XP_011532172.1:p.Phe246Ser
XM_011533871.1:c.608T>C	XP_011532173.1:p.Phe203Ser
NM_001354798.1:c.626-1826T>C	NP_001341727.1:n.626-1826T>C
NM_017875.4:c.788T>C MANE Select	NP_060345.2:p.Phe263Ser
XM_006713214.2:c.776T>C	XP_006713277.1:p.Phe259Ser
XM_011533869.2:c.770T>C	XP_011532171.1:p.Phe257Ser
XM_024453611.1:c.734T>C	XP_024309379.1:p.Phe245Ser
NM_001354798.2:c.626-1826T>C	NP_001341727.1:n.626-1826T>C