Canonical Allele Identifier: CA9200710

Gene: DNM2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10759722T>C , CM000681.2:g.10759722T>C	GRCh38
NC_000019.9:g.10870398T>C , CM000681.1:g.10870398T>C	GRCh37
NC_000019.8:g.10731398T>C	NCBI36
NG_008792.1:g.46644T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682285.1:n.350-16T>C
ENST00000682524.1:n.350-16T>C
ENST00000683738.1:n.350-16T>C
ENST00000355667.11:c.162-16T>C	ENSP00000347890.6:n.162-16T>C
ENST00000389253.9:c.162-16T>C MANE Select	ENSP00000373905.4:n.162-16T>C
ENST00000355667.10:c.162-16T>C	ENSP00000347890.6:n.162-16T>C
ENST00000359692.10:c.162-16T>C	ENSP00000352721.6:n.162-16T>C
ENST00000389253.8:c.162-16T>C	ENSP00000373905.3:n.162-16T>C
ENST00000408974.8:c.162-16T>C	ENSP00000386192.3:n.162-16T>C
ENST00000585892.5:c.162-16T>C	ENSP00000468734.1:n.162-16T>C
ENST00000586939.5:c.-313-16T>C	ENSP00000467430.1:n.-313-16T>C
ENST00000588976.1:n.457T>C
NM_001005360.2:c.162-16T>C	NP_001005360.1:n.162-16T>C
NM_001005361.2:c.162-16T>C	NP_001005361.1:n.162-16T>C
NM_001005362.2:c.162-16T>C	NP_001005362.1:n.162-16T>C
NM_001190716.1:c.162-16T>C	NP_001177645.1:n.162-16T>C
NM_004945.3:c.162-16T>C	NP_004936.2:n.162-16T>C
NM_001005361.3:c.162-16T>C MANE Select	NP_001005361.1:n.162-16T>C
NM_001190716.2:c.162-16T>C	NP_001177645.1:n.162-16T>C
NM_001005360.3:c.162-16T>C	NP_001005360.1:n.162-16T>C
NM_001005362.3:c.162-16T>C	NP_001005362.1:n.162-16T>C
NM_004945.4:c.162-16T>C	NP_004936.2:n.162-16T>C