Canonical Allele Identifier: CA11924864

Gene: DROSHA

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.31413042A>G , CM000667.2:g.31413042A>G	GRCh38
NC_000005.9:g.31413149A>G , CM000667.1:g.31413149A>G	GRCh37
NC_000005.8:g.31448906A>G	NCBI36
NG_051574.1:g.124134T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344624.8:c.3526-2155T>C MANE Select	ENSP00000339845.3:n.3526-2155T>C
ENST00000344624.7:c.3526-2155T>C	ENSP00000339845.3:n.3526-2155T>C
ENST00000442743.5:c.3415-2155T>C	ENSP00000409335.1:n.3415-2155T>C
ENST00000511367.6:c.3526-2155T>C	ENSP00000425979.2:n.3526-2155T>C
ENST00000511778.5:n.642-2155T>C
ENST00000513349.5:c.3415-2155T>C	ENSP00000424161.1:n.3415-2155T>C
NM_001100412.1:c.3415-2155T>C	NP_001093882.1:n.3415-2155T>C
NM_013235.4:c.3526-2155T>C	NP_037367.3:n.3526-2155T>C
XM_005248291.2:c.3526-2155T>C	XP_005248348.1:n.3526-2155T>C
XM_005248292.2:c.3502-2155T>C	XP_005248349.1:n.3502-2155T>C
XM_005248293.2:c.3433-2155T>C	XP_005248350.1:n.3433-2155T>C
XM_005248294.2:c.3322-2155T>C	XP_005248351.1:n.3322-2155T>C
XM_011514033.1:c.3526-2155T>C	XP_011512335.1:n.3526-2155T>C
XM_005248291.4:c.3526-2155T>C	XP_005248348.1:n.3526-2155T>C
XM_005248292.4:c.3502-2155T>C	XP_005248349.1:n.3502-2155T>C
XM_005248293.4:c.3433-2155T>C	XP_005248350.1:n.3433-2155T>C
XM_005248294.4:c.3322-2155T>C	XP_005248351.1:n.3322-2155T>C
XM_011514033.3:c.3526-2155T>C	XP_011512335.1:n.3526-2155T>C
XM_017009399.2:c.3409-2155T>C	XP_016864888.1:n.3409-2155T>C
XM_017009400.2:c.3391-2155T>C	XP_016864889.1:n.3391-2155T>C
XM_017009401.2:c.3298-2155T>C	XP_016864890.1:n.3298-2155T>C
XM_017009402.1:c.1822-2155T>C	XP_016864891.1:n.1822-2155T>C
XM_024446033.1:c.3526-2155T>C	XP_024301801.1:n.3526-2155T>C
XM_024446034.1:c.3526-2155T>C	XP_024301802.1:n.3526-2155T>C
XM_024446035.1:c.3415-2155T>C	XP_024301803.1:n.3415-2155T>C
NM_001100412.2:c.3415-2155T>C	NP_001093882.1:n.3415-2155T>C
NM_013235.5:c.3526-2155T>C	NP_037367.3:n.3526-2155T>C
NM_001382508.1:c.3526-2155T>C MANE Select	NP_001369437.1:n.3526-2155T>C