Canonical Allele Identifier: CA1540679647

Gene: DAB2 C9

Linked Data

• dbSNP Id: rs2255280

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.39394887C>T , CM000667.2:g.39394887C>T	GRCh38
NC_000005.9:g.39394989C>T , CM000667.1:g.39394989C>T	GRCh37
NC_000005.8:g.39430746C>T	NCBI36
NG_030312.1:g.35347G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000320816.11:c.-101-466G>A (DAB2) MANE Select	ENSP00000313391.6:n.-101-466G>A
ENST00000320816.10:c.-101-466G>A (DAB2)	ENSP00000313391.6:n.-101-466G>A
ENST00000339788.10:c.-101-466G>A (DAB2)	ENSP00000345508.6:n.-101-466G>A
ENST00000483232.6:n.66-6035G>A (C9)
ENST00000503513.5:c.-101-466G>A (DAB2)	ENSP00000425088.1:n.-101-466G>A
ENST00000507539.5:c.-101-466G>A (DAB2)	ENSP00000421526.1:n.-101-466G>A
ENST00000511792.5:c.-101-466G>A (DAB2)	ENSP00000427541.1:n.-101-466G>A
ENST00000513052.1:n.458-466G>A (DAB2)
ENST00000515269.5:n.233-466G>A (DAB2)
ENST00000515700.5:c.-101-466G>A (DAB2)	ENSP00000421086.1:n.-101-466G>A
ENST00000545653.5:c.-101-466G>A (DAB2)	ENSP00000439919.1:n.-101-466G>A
NM_001244871.1:c.-101-466G>A (DAB2)	NP_001231800.1:n.-101-466G>A
NM_001343.3:c.-101-466G>A (DAB2)	NP_001334.2:n.-101-466G>A
NM_001343.4:c.-101-466G>A (DAB2) MANE Select	NP_001334.2:n.-101-466G>A
NM_001244871.2:c.-101-466G>A (DAB2)	NP_001231800.1:n.-101-466G>A