Canonical Allele Identifier: CA139736109

Gene: RAB23

Linked Data

• dbSNP Id: rs774712631
• MyVariant Identifiers: chr6:g.57054859del (hg19) ; chr6:g.57190061del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.57190064del , CM000668.2:g.57190064del	GRCh38
NC_000006.11:g.57054862del , CM000668.1:g.57054862del	GRCh37
NC_000006.10:g.57162821del	NCBI36
NG_012170.1:g.37220del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468148.6:c.*400del MANE Select	ENSP00000417610.1:n.*400del
ENST00000317483.4:c.*400del	ENSP00000320413.3:n.*400del
ENST00000468148.5:c.*400del	ENSP00000417610.1:n.*400del
NM_001278666.1:c.*400del	NP_001265595.1:n.*400del
NM_001278667.1:c.*400del	NP_001265596.1:n.*400del
NM_001278668.1:c.*400del	NP_001265597.1:n.*400del
NM_016277.4:c.*400del	NP_057361.3:n.*400del
NM_183227.2:c.*400del	NP_899050.1:n.*400del
NR_103822.1:n.973del
NM_016277.5:c.*400del MANE Select	NP_057361.3:n.*400del
NM_001278666.2:c.*400del	NP_001265595.1:n.*400del
NM_001278667.2:c.*400del	NP_001265596.1:n.*400del
NM_001278668.2:c.*400del	NP_001265597.1:n.*400del
NM_183227.3:c.*400del	NP_899050.1:n.*400del
NR_103822.2:n.966del