Canonical Allele Identifier: CA792209307

Gene: SLC25A4

Linked Data

• dbSNP Id: rs34795113
• MyVariant Identifiers: chr4:g.186065845_186065847del (hg19) ; chr4:g.185144691_185144693del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.185144697_185144699del , CM000666.2:g.185144697_185144699del	GRCh38
NC_000004.11:g.186065851_186065853del , CM000666.1:g.186065851_186065853del	GRCh37
NC_000004.10:g.186302845_186302847del	NCBI36
NG_013001.1:g.6435_6437del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281456.11:c.112-67_112-65del MANE Select	ENSP00000281456.5:n.112-67_112-65del
ENST00000281456.10:c.112-67_112-65del	ENSP00000281456.5:n.112-67_112-65del
ENST00000491736.1:c.112-67_112-65del	ENSP00000476711.1:n.112-67_112-65del
NM_001151.3:c.112-67_112-65del	NP_001142.2:n.112-67_112-65del
NM_001151.4:c.112-67_112-65del MANE Select	NP_001142.2:n.112-67_112-65del