Canonical Allele Identifier: CA390332154

Gene: DNAL1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.73687290G>A , CM000676.2:g.73687290G>A	GRCh38
NC_000014.8:g.74153993G>A , CM000676.1:g.74153993G>A	GRCh37
NC_000014.7:g.73223746G>A	NCBI36
NG_028083.1:g.47416G>A
NG_028083.2:g.47416G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_031427.4:c.296G>A MANE Select	NP_113615.2:p.Trp99Ter
ENST00000553645.7:c.296G>A MANE Select	ENSP00000452037.1:p.Trp99Ter
NM_001201366.1:c.179G>A	NP_001188295.1:p.Trp60Ter
NM_001201366.2:c.179G>A	NP_001188295.1:p.Trp60Ter
NM_031427.3:c.296G>A	NP_113615.2:p.Trp99Ter
ENST00000311089.7:c.-44G>A	ENSP00000310360.3:n.-44G>A
ENST00000553645.6:c.296G>A	ENSP00000452037.1:p.Trp99Ter
ENST00000554113.5:c.-44G>A	ENSP00000452368.1:n.-44G>A
ENST00000554159.1:c.183G>A	ENSP00000451264.1:p.Val61=
ENST00000554339.5:c.35G>A	ENSP00000450744.1:p.Trp12Ter
ENST00000554871.5:c.179G>A	ENSP00000451834.1:p.Trp60Ter
ENST00000555631.6:c.179G>A	ENSP00000451547.2:p.Trp60Ter
ENST00000559993.1:c.-44G>A	ENSP00000453439.1:n.-44G>A
XM_011537204.1:c.179G>A	XP_011535506.1:p.Trp60Ter
XM_017021679.2:c.179G>A	XP_016877168.1:p.Trp60Ter
XM_024449715.1:c.179G>A	XP_024305483.1:p.Trp60Ter