Canonical Allele Identifier: CA352204393

Gene: SLC25A38

Linked Data

• gnomAD v4: 3-39394412-C-T
• MyVariant Identifiers: chr3:g.39435903C>T (hg19) ; chr3:g.39394412C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394412C>T , CM000665.2:g.39394412C>T	GRCh38
NC_000003.11:g.39435903C>T , CM000665.1:g.39435903C>T	GRCh37
NC_000003.10:g.39410907C>T	NCBI36
NG_016931.1:g.16089C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.580C>T	ENSP00000495376.1:p.Gln194Ter
ENST00000643672.1:c.577C>T	ENSP00000494532.1:p.Gln193Ter
ENST00000645280.1:c.574C>T	ENSP00000496690.1:p.Gln192Ter
ENST00000645630.1:c.448C>T	ENSP00000493714.1:p.Gln150Ter
ENST00000648579.1:c.722-38C>T	ENSP00000497638.1:n.722-38C>T
ENST00000650617.1:c.628C>T MANE Select	ENSP00000497532.1:p.Gln210Ter
ENST00000273158.8:c.628C>T	ENSP00000273158.3:p.Gln210Ter
NM_017875.2:c.628C>T	NP_060345.2:p.Gln210Ter
XM_006713214.1:c.616C>T	XP_006713277.1:p.Gln206Ter
XM_011533869.1:c.610C>T	XP_011532171.1:p.Gln204Ter
XM_011533870.1:c.577C>T	XP_011532172.1:p.Gln193Ter
XM_011533871.1:c.448C>T	XP_011532173.1:p.Gln150Ter
NM_001354798.1:c.626-1986C>T	NP_001341727.1:n.626-1986C>T
NM_017875.4:c.628C>T MANE Select	NP_060345.2:p.Gln210Ter
XM_006713214.2:c.616C>T	XP_006713277.1:p.Gln206Ter
XM_011533869.2:c.610C>T	XP_011532171.1:p.Gln204Ter
XM_024453611.1:c.574C>T	XP_024309379.1:p.Gln192Ter
NM_001354798.2:c.626-1986C>T	NP_001341727.1:n.626-1986C>T