Canonical Allele Identifier: CA364625470

Gene: RAB23

Linked Data

• MyVariant Identifiers: chr6:g.57055374C>A (hg19) ; chr6:g.57190576C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.57190576C>A , CM000668.2:g.57190576C>A	GRCh38
NC_000006.11:g.57055374C>A , CM000668.1:g.57055374C>A	GRCh37
NC_000006.10:g.57163333C>A	NCBI36
NG_012170.1:g.36705G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468148.6:c.599G>T MANE Select	ENSP00000417610.1:p.Ser200Ile
ENST00000317483.4:c.599G>T	ENSP00000320413.3:p.Ser200Ile
ENST00000468148.5:c.599G>T	ENSP00000417610.1:p.Ser200Ile
NM_001278666.1:c.599G>T	NP_001265595.1:p.Ser200Ile
NM_001278667.1:c.599G>T	NP_001265596.1:p.Ser200Ile
NM_001278668.1:c.599G>T	NP_001265597.1:p.Ser200Ile
NM_016277.4:c.599G>T	NP_057361.3:p.Ser200Ile
NM_183227.2:c.599G>T	NP_899050.1:p.Ser200Ile
NR_103822.1:n.458G>T
NM_016277.5:c.599G>T MANE Select	NP_057361.3:p.Ser200Ile
NM_001278666.2:c.599G>T	NP_001265595.1:p.Ser200Ile
NM_001278667.2:c.599G>T	NP_001265596.1:p.Ser200Ile
NM_001278668.2:c.599G>T	NP_001265597.1:p.Ser200Ile
NM_183227.3:c.599G>T	NP_899050.1:p.Ser200Ile
NR_103822.2:n.451G>T