Canonical Allele Identifier: CA358896195
Gene: SLC25A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144894A>G , CM000666.2:g.185144894A>G GRCh38
NC_000004.11:g.186066048A>G , CM000666.1:g.186066048A>G GRCh37
NC_000004.10:g.186303042A>G NCBI36
NG_013001.1:g.6632A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.242A>G MANE Select ENSP00000281456.5:p.Tyr81Cys
ENST00000281456.10:c.242A>G ENSP00000281456.5:p.Tyr81Cys
ENST00000491736.1:c.242A>G ENSP00000476711.1:p.Tyr81Cys
NM_001151.3:c.242A>G NP_001142.2:p.Tyr81Cys
NM_001151.4:c.242A>G MANE Select NP_001142.2:p.Tyr81Cys