Canonical Allele Identifier: CA906962558

Gene: SLC25A38

Linked Data

• dbSNP Id: rs1453093600
• gnomAD v3: 3-39397014-C-T
• gnomAD v4: 3-39397014-C-T
• MyVariant Identifiers: chr3:g.39438505C>T (hg19) ; chr3:g.39397014C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39397014C>T , CM000665.2:g.39397014C>T	GRCh38
NC_000003.11:g.39438505C>T , CM000665.1:g.39438505C>T	GRCh37
NC_000003.10:g.39413509C>T	NCBI36
NG_016931.1:g.18691C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648579.1:c.*706C>T	ENSP00000497638.1:n.*706C>T
ENST00000650617.1:c.*494C>T MANE Select	ENSP00000497532.1:n.*494C>T
ENST00000273158.8:c.*494C>T	ENSP00000273158.3:n.*494C>T
NM_017875.2:c.*494C>T	NP_060345.2:n.*494C>T
XM_006713214.1:c.*494C>T	XP_006713277.1:n.*494C>T
XM_011533869.1:c.*494C>T	XP_011532171.1:n.*494C>T
XM_011533870.1:c.*494C>T	XP_011532172.1:n.*494C>T
XM_011533871.1:c.*494C>T	XP_011532173.1:n.*494C>T
NM_001354798.1:c.*528C>T	NP_001341727.1:n.*528C>T
NM_017875.4:c.*494C>T MANE Select	NP_060345.2:n.*494C>T
XM_006713214.2:c.*494C>T	XP_006713277.1:n.*494C>T
XM_011533869.2:c.*494C>T	XP_011532171.1:n.*494C>T
XM_024453611.1:c.*494C>T	XP_024309379.1:n.*494C>T
NM_001354798.2:c.*528C>T	NP_001341727.1:n.*528C>T