Canonical Allele Identifier: CA1519346851

Gene: SLC25A4

Linked Data

• dbSNP Id: rs1734405636
• gnomAD v4: 4-185144689-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.185144690_185144691del , CM000666.2:g.185144690_185144691del	GRCh38
NC_000004.11:g.186065844_186065845del , CM000666.1:g.186065844_186065845del	GRCh37
NC_000004.10:g.186302838_186302839del	NCBI36
NG_013001.1:g.6428_6429del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281456.11:c.112-74_112-73del MANE Select	ENSP00000281456.5:n.112-74_112-73del
ENST00000281456.10:c.112-74_112-73del	ENSP00000281456.5:n.112-74_112-73del
ENST00000491736.1:c.112-74_112-73del	ENSP00000476711.1:n.112-74_112-73del
NM_001151.3:c.112-74_112-73del	NP_001142.2:n.112-74_112-73del
NM_001151.4:c.112-74_112-73del MANE Select	NP_001142.2:n.112-74_112-73del