Canonical Allele Identifier: CA2658200542

Gene: RAB10

Linked Data

• gnomAD v4: 2-26135167-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26135167C>T , CM000664.2:g.26135167C>T	GRCh38
NC_000002.11:g.26358036C>T , CM000664.1:g.26358036C>T	GRCh37
NC_000002.10:g.26211540C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264710.5:c.*146C>T MANE Select	ENSP00000264710.4:n.*146C>T
ENST00000264710.4:c.*146C>T	ENSP00000264710.4:n.*146C>T
ENST00000495146.5:n.1112C>T
NM_016131.4:c.*146C>T	NP_057215.3:n.*146C>T
XM_024452565.1:c.*146C>T	XP_024308333.1:n.*146C>T
NM_016131.5:c.*146C>T MANE Select	NP_057215.3:n.*146C>T