Canonical Allele Identifier: CA358896066

Gene: SLC25A4

Linked Data

• MyVariant Identifiers: chr4:g.186065991C>G (hg19) ; chr4:g.185144837C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.185144837C>G , CM000666.2:g.185144837C>G	GRCh38
NC_000004.11:g.186065991C>G , CM000666.1:g.186065991C>G	GRCh37
NC_000004.10:g.186302985C>G	NCBI36
NG_013001.1:g.6575C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281456.11:c.185C>G MANE Select	ENSP00000281456.5:p.Pro62Arg
ENST00000281456.10:c.185C>G	ENSP00000281456.5:p.Pro62Arg
ENST00000491736.1:c.185C>G	ENSP00000476711.1:p.Pro62Arg
NM_001151.3:c.185C>G	NP_001142.2:p.Pro62Arg
NM_001151.4:c.185C>G MANE Select	NP_001142.2:p.Pro62Arg