Canonical Allele Identifier: CA117195745
Gene: DAB2 HGNC NCBI
C9 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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