Canonical Allele Identifier: CA208194371

Gene: DNA2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68422611A>G , CM000672.2:g.68422611A>G	GRCh38
NC_000010.10:g.70182368A>G , CM000672.1:g.70182368A>G	GRCh37
NC_000010.9:g.69852374A>G	NCBI36
NG_034247.1:g.54363T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001080449.3:c.2403-7T>C MANE Select	NP_001073918.2:n.2403-7T>C
ENST00000358410.8:c.2403-7T>C MANE Select	ENSP00000351185.3:n.2403-7T>C
NM_001080449.2:c.2403-7T>C	NP_001073918.2:n.2403-7T>C
NR_102264.1:n.2377-7T>C
NR_102264.2:n.2377-7T>C
ENST00000358410.7:c.2403-7T>C	ENSP00000351185.3:n.2403-7T>C
ENST00000399179.6:c.*224-7T>C	ENSP00000382132.3:n.*224-7T>C
ENST00000399180.3:c.*224-7T>C	ENSP00000382133.3:n.*224-7T>C
ENST00000440722.2:c.367-7T>C
ENST00000551118.6:c.1984-2719T>C	ENSP00000450393.3:n.1984-2719T>C
XM_006717680.2:c.2493-7T>C	XP_006717743.1:n.2493-7T>C
XM_006717680.3:c.2493-7T>C	XP_006717743.1:n.2493-7T>C
XM_011539416.1:c.2493-7T>C	XP_011537718.1:n.2493-7T>C
XM_011539417.1:c.1323-7T>C	XP_011537719.1:n.1323-7T>C
XM_017015799.1:c.1731-7T>C	XP_016871288.1:n.1731-7T>C