Canonical Allele Identifier: CA1537049233

Gene: DROSHA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.31401336_31401344delinsCTTCATTCA , CM000667.2:g.31401336_31401344delinsCTTCATTCA	GRCh38
NC_000005.9:g.31401443_31401451delinsCTTCATTCA , CM000667.1:g.31401443_31401451delinsCTTCATTCA	GRCh37
NC_000005.8:g.31437200_31437208delinsCTTCATTCA	NCBI36
NG_051574.1:g.135832_135840delinsTGAATGAAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000344624.8:c.*88_*96delinsTGAATGAAG MANE Select	ENSP00000339845.3:n.*88_*96delinsTGAATGAAG
ENST00000344624.7:c.*88_*96delinsTGAATGAAG	ENSP00000339845.3:n.*88_*96delinsTGAATGAAG
ENST00000442743.5:c.*88_*96delinsTGAATGAAG	ENSP00000409335.1:n.*88_*96delinsTGAATGAAG
ENST00000511367.6:c.*88_*96delinsTGAATGAAG	ENSP00000425979.2:n.*88_*96delinsTGAATGAAG
ENST00000513349.5:c.*88_*96delinsTGAATGAAG	ENSP00000424161.1:n.*88_*96delinsTGAATGAAG
ENST00000514927.6:n.370_378delinsTGAATGAAG
NM_001100412.1:c.*88_*96delinsTGAATGAAG	NP_001093882.1:n.*88_*96delinsTGAATGAAG
NM_013235.4:c.*88_*96delinsTGAATGAAG	NP_037367.3:n.*88_*96delinsTGAATGAAG
XM_005248291.2:c.*88_*96delinsTGAATGAAG	XP_005248348.1:n.*88_*96delinsTGAATGAAG
XM_005248292.2:c.*88_*96delinsTGAATGAAG	XP_005248349.1:n.*88_*96delinsTGAATGAAG
XM_005248293.2:c.*88_*96delinsTGAATGAAG	XP_005248350.1:n.*88_*96delinsTGAATGAAG
XM_005248294.2:c.*88_*96delinsTGAATGAAG	XP_005248351.1:n.*88_*96delinsTGAATGAAG
XM_005248291.4:c.*88_*96delinsTGAATGAAG	XP_005248348.1:n.*88_*96delinsTGAATGAAG
XM_005248292.4:c.*88_*96delinsTGAATGAAG	XP_005248349.1:n.*88_*96delinsTGAATGAAG
XM_005248293.4:c.*88_*96delinsTGAATGAAG	XP_005248350.1:n.*88_*96delinsTGAATGAAG
XM_005248294.4:c.*88_*96delinsTGAATGAAG	XP_005248351.1:n.*88_*96delinsTGAATGAAG
XM_017009399.2:c.*88_*96delinsTGAATGAAG	XP_016864888.1:n.*88_*96delinsTGAATGAAG
XM_017009400.2:c.*88_*96delinsTGAATGAAG	XP_016864889.1:n.*88_*96delinsTGAATGAAG
XM_017009401.2:c.*88_*96delinsTGAATGAAG	XP_016864890.1:n.*88_*96delinsTGAATGAAG
XM_017009402.1:c.*88_*96delinsTGAATGAAG	XP_016864891.1:n.*88_*96delinsTGAATGAAG
XM_024446033.1:c.*88_*96delinsTGAATGAAG	XP_024301801.1:n.*88_*96delinsTGAATGAAG
XM_024446034.1:c.*88_*96delinsTGAATGAAG	XP_024301802.1:n.*88_*96delinsTGAATGAAG
XM_024446035.1:c.*88_*96delinsTGAATGAAG	XP_024301803.1:n.*88_*96delinsTGAATGAAG
NM_001100412.2:c.*88_*96delinsTGAATGAAG	NP_001093882.1:n.*88_*96delinsTGAATGAAG
NM_013235.5:c.*88_*96delinsTGAATGAAG	NP_037367.3:n.*88_*96delinsTGAATGAAG
NM_001382508.1:c.*88_*96delinsTGAATGAAG MANE Select	NP_001369437.1:n.*88_*96delinsTGAATGAAG