Canonical Allele Identifier: CA2679243913

Gene: RAB23

Linked Data

• gnomAD v4: 6-57190060-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.57190060G>T , CM000668.2:g.57190060G>T	GRCh38
NC_000006.11:g.57054858G>T , CM000668.1:g.57054858G>T	GRCh37
NC_000006.10:g.57162817G>T	NCBI36
NG_012170.1:g.37221C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468148.6:c.*401C>A MANE Select	ENSP00000417610.1:n.*401C>A
ENST00000317483.4:c.*401C>A	ENSP00000320413.3:n.*401C>A
ENST00000468148.5:c.*401C>A	ENSP00000417610.1:n.*401C>A
NM_001278666.1:c.*401C>A	NP_001265595.1:n.*401C>A
NM_001278667.1:c.*401C>A	NP_001265596.1:n.*401C>A
NM_001278668.1:c.*401C>A	NP_001265597.1:n.*401C>A
NM_016277.4:c.*401C>A	NP_057361.3:n.*401C>A
NM_183227.2:c.*401C>A	NP_899050.1:n.*401C>A
NR_103822.1:n.974C>A
NM_016277.5:c.*401C>A MANE Select	NP_057361.3:n.*401C>A
NM_001278666.2:c.*401C>A	NP_001265595.1:n.*401C>A
NM_001278667.2:c.*401C>A	NP_001265596.1:n.*401C>A
NM_001278668.2:c.*401C>A	NP_001265597.1:n.*401C>A
NM_183227.3:c.*401C>A	NP_899050.1:n.*401C>A
NR_103822.2:n.967C>A