Canonical Allele Identifier: CA741748972

Gene: DSTN

Linked Data

• dbSNP Id: rs1253081832
• MyVariant Identifiers: chr20:g.17566014_17566017del (hg19) ; chr20:g.17585369_17585372del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.17585372_17585375del , CM000682.2:g.17585372_17585375del	GRCh38
NC_000020.10:g.17566017_17566020del , CM000682.1:g.17566017_17566020del	GRCh37
NC_000020.9:g.17514017_17514020del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000246069.12:c.3+15161_3+15164del MANE Select	ENSP00000246069.6:n.3+15161_3+15164del
ENST00000246069.11:c.3+15161_3+15164del	ENSP00000246069.6:n.3+15161_3+15164del
ENST00000449141.2:c.3+15161_3+15164del	ENSP00000434355.1:n.3+15161_3+15164del
ENST00000474024.5:c.-180-6560_-180-6557del	ENSP00000476975.1:n.-180-6560_-180-6557de...
NM_001011546.1:c.-180-6560_-180-6557del	NP_001011546.1:n.-180-6560_-180-6557del
NM_006870.3:c.3+15161_3+15164del	NP_006861.1:n.3+15161_3+15164del
XM_011529142.1:c.3+15161_3+15164del	XP_011527444.1:n.3+15161_3+15164del
XM_011529143.1:c.3+15161_3+15164del	XP_011527445.1:n.3+15161_3+15164del
XM_011529144.1:c.-180-6560_-180-6557del	XP_011527446.1:n.-180-6560_-180-6557del
NM_006870.4:c.3+15161_3+15164del MANE Select	NP_006861.1:n.3+15161_3+15164del
NM_001011546.2:c.-180-6560_-180-6557del	NP_001011546.1:n.-180-6560_-180-6557del