Canonical Allele Identifier: CA2711533992

Gene: RAB23 BAG2

Linked Data

• dbSNP Id: rs1458997816

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.57189499G>A , CM000668.2:g.57189499G>A	GRCh38
NC_000006.11:g.57054297G>A , CM000668.1:g.57054297G>A	GRCh37
NC_000006.10:g.57162256G>A	NCBI36
NG_012170.1:g.37782C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000468148.6:c.*962C>T (RAB23) MANE Select	ENSP00000417610.1:n.*962C>T
ENST00000317483.4:c.*962C>T (RAB23)	ENSP00000320413.3:n.*962C>T
ENST00000370693.5:c.*5309G>A (BAG2) MANE Select	ENSP00000359727.4:n.*5309G>A
ENST00000468148.5:c.*962C>T (RAB23)	ENSP00000417610.1:n.*962C>T
NM_001278666.1:c.*962C>T (RAB23)	NP_001265595.1:n.*962C>T
NM_001278667.1:c.*962C>T (RAB23)	NP_001265596.1:n.*962C>T
NM_001278668.1:c.*962C>T (RAB23)	NP_001265597.1:n.*962C>T
NM_016277.4:c.*962C>T (RAB23)	NP_057361.3:n.*962C>T
NM_183227.2:c.*962C>T (RAB23)	NP_899050.1:n.*962C>T
NR_103822.1:n.1535C>T (RAB23)
NM_004282.4:c.*5309G>A (BAG2) MANE Select	NP_004273.1:n.*5309G>A
NM_016277.5:c.*962C>T (RAB23) MANE Select	NP_057361.3:n.*962C>T
NM_001278666.2:c.*962C>T (RAB23)	NP_001265595.1:n.*962C>T
NM_001278667.2:c.*962C>T (RAB23)	NP_001265596.1:n.*962C>T
NM_001278668.2:c.*962C>T (RAB23)	NP_001265597.1:n.*962C>T
NM_183227.3:c.*962C>T (RAB23)	NP_899050.1:n.*962C>T
NR_103822.2:n.1528C>T (RAB23)