Canonical Allele Identifier: CA2341294841

Gene: CD33

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.51239889G>T , CM000681.2:g.51239889G>T	GRCh38
NC_000019.9:g.51743144G>T , CM000681.1:g.51743144G>T	GRCh37
NC_000019.8:g.56434956G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262262.5:c.*201G>T MANE Select	ENSP00000262262.3:n.*201G>T
ENST00000262262.4:c.*201G>T	ENSP00000262262.3:n.*201G>T
ENST00000421133.6:c.*201G>T	ENSP00000410126.1:n.*201G>T
ENST00000598473.1:n.4211+151G>T
ENST00000600557.1:n.410G>T
ENST00000601785.5:n.1423G>T
NM_001082618.1:c.*201G>T	NP_001076087.1:n.*201G>T
NM_001772.3:c.*201G>T	NP_001763.3:n.*201G>T
XM_011527531.1:c.*201G>T	XP_011525833.1:n.*201G>T
XM_011527532.1:c.*201G>T	XP_011525834.1:n.*201G>T
XR_935875.1:n.1883G>T
XM_011527531.2:c.*201G>T	XP_011525833.1:n.*201G>T
XM_011527532.2:c.*201G>T	XP_011525834.1:n.*201G>T
XM_017027508.1:c.*201G>T	XP_016882997.1:n.*201G>T
XM_017027509.1:c.*201G>T	XP_016882998.1:n.*201G>T
XM_017027510.1:c.*201G>T	XP_016882999.1:n.*201G>T
NM_001772.4:c.*201G>T MANE Select	NP_001763.3:n.*201G>T
NM_001082618.2:c.*201G>T	NP_001076087.1:n.*201G>T