Canonical Allele Identifier: CA28978181

Gene: DCLRE1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113907234T>A , CM000663.2:g.113907234T>A	GRCh38
NC_000001.10:g.114449856T>A , CM000663.1:g.114449856T>A	GRCh37
NC_000001.9:g.114251379T>A	NCBI36
NG_031901.1:g.2886A>T
NG_057565.1:g.7616T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_022836.4:c.355+73T>A MANE Select	NP_073747.1:n.355+73T>A
ENST00000650450.2:c.355+73T>A MANE Select	ENSP00000498042.1:n.355+73T>A
NM_001319946.2:c.-23-775T>A	NP_001306875.1:n.-23-775T>A
NM_001319947.2:c.-23-775T>A	NP_001306876.1:n.-23-775T>A
NM_001363690.1:c.355+73T>A	NP_001350619.1:n.355+73T>A
NM_001363690.2:c.355+73T>A	NP_001350619.1:n.355+73T>A
NM_001363691.1:c.-23-775T>A	NP_001350620.1:n.-23-775T>A
NM_001363691.2:c.-23-775T>A	NP_001350620.1:n.-23-775T>A
NM_022836.3:c.355+73T>A	NP_073747.1:n.355+73T>A
ENST00000369563.3:c.355+73T>A	ENSP00000358576.3:n.355+73T>A
ENST00000466480.1:n.368-775T>A
ENST00000466480.2:c.190-775T>A	ENSP00000497696.1:n.190-775T>A
ENST00000648795.1:c.190-775T>A	ENSP00000497557.1:n.190-775T>A
ENST00000650596.1:c.355+73T>A	ENSP00000497882.1:n.355+73T>A
ENST00000697125.1:n.398-775T>A
XM_005271130.2:c.-23-775T>A	XP_005271187.1:n.-23-775T>A