Canonical Allele Identifier: CA2838276397

Gene: DPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43970155C>A , CM000663.2:g.43970155C>A	GRCh38
NC_000001.10:g.44435827C>A , CM000663.1:g.44435827C>A	GRCh37
NC_000001.9:g.44208414C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255108.8:c.-21C>A MANE Select	ENSP00000255108.3:n.-21C>A
ENST00000255108.7:c.-21C>A	ENSP00000255108.3:n.-21C>A
ENST00000396758.6:c.-21C>A	ENSP00000379981.2:n.-21C>A
ENST00000471934.1:n.156C>A
ENST00000476260.1:c.-21C>A	ENSP00000436330.1:n.-21C>A
ENST00000477294.5:n.127C>A
ENST00000490861.5:n.132C>A
ENST00000492306.5:c.-21C>A	ENSP00000433273.1:n.-21C>A
ENST00000495421.1:c.-21C>A	ENSP00000431944.1:n.-21C>A
ENST00000524776.5:c.-21C>A	ENSP00000434977.1:n.-21C>A
ENST00000527567.1:n.133C>A
ENST00000529729.1:n.127C>A
ENST00000530988.1:n.146C>A
ENST00000532140.1:c.-21C>A	ENSP00000431831.1:n.-21C>A
ENST00000534786.1:n.51C>A
NM_001039589.1:c.-21C>A	NP_001034678.1:n.-21C>A
NM_001384.4:c.-21C>A	NP_001375.2:n.-21C>A
XM_005270559.2:c.-197C>A	XP_005270616.1:n.-197C>A
XM_011540866.1:c.-660C>A	XP_011539168.1:n.-660C>A
XM_011540867.1:c.-608C>A	XP_011539169.1:n.-608C>A
NM_001319165.1:c.-239C>A	NP_001306094.1:n.-239C>A
NM_001319166.1:c.-21C>A	NP_001306095.1:n.-21C>A
NM_001319167.1:c.-657C>A	NP_001306096.1:n.-657C>A
NM_001319168.1:c.-197C>A	NP_001306097.1:n.-197C>A
NM_001319169.1:c.-202C>A	NP_001306098.1:n.-202C>A
NM_001319170.1:c.-660C>A	NP_001306099.1:n.-660C>A
NM_001319171.1:c.-496C>A	NP_001306100.1:n.-496C>A
XM_017000502.2:c.-21C>A	XP_016855991.1:n.-21C>A
NM_001384.5:c.-21C>A MANE Select	NP_001375.2:n.-21C>A
NM_001039589.2:c.-21C>A	NP_001034678.1:n.-21C>A
NM_001319165.2:c.-239C>A	NP_001306094.1:n.-239C>A
NM_001319166.2:c.-21C>A	NP_001306095.1:n.-21C>A
NM_001319167.2:c.-657C>A	NP_001306096.1:n.-657C>A
NM_001319168.2:c.-197C>A	NP_001306097.1:n.-197C>A
NM_001319169.2:c.-202C>A	NP_001306098.1:n.-202C>A
NM_001319170.2:c.-660C>A	NP_001306099.1:n.-660C>A
NM_001319171.2:c.-496C>A	NP_001306100.1:n.-496C>A