Canonical Allele Identifier: CA1015849350

Gene: DSTN

Linked Data

• dbSNP Id: rs2035393739
• gnomAD v3: 20-17585351-G-C
• gnomAD v4: 20-17585351-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.17585351G>C , CM000682.2:g.17585351G>C	GRCh38
NC_000020.10:g.17565996G>C , CM000682.1:g.17565996G>C	GRCh37
NC_000020.9:g.17513996G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000246069.12:c.3+15140G>C MANE Select	ENSP00000246069.6:n.3+15140G>C
ENST00000246069.11:c.3+15140G>C	ENSP00000246069.6:n.3+15140G>C
ENST00000449141.2:c.3+15140G>C	ENSP00000434355.1:n.3+15140G>C
ENST00000474024.5:c.-180-6581G>C	ENSP00000476975.1:n.-180-6581G>C
NM_001011546.1:c.-180-6581G>C	NP_001011546.1:n.-180-6581G>C
NM_006870.3:c.3+15140G>C	NP_006861.1:n.3+15140G>C
XM_011529142.1:c.3+15140G>C	XP_011527444.1:n.3+15140G>C
XM_011529143.1:c.3+15140G>C	XP_011527445.1:n.3+15140G>C
XM_011529144.1:c.-180-6581G>C	XP_011527446.1:n.-180-6581G>C
NM_006870.4:c.3+15140G>C MANE Select	NP_006861.1:n.3+15140G>C
NM_001011546.2:c.-180-6581G>C	NP_001011546.1:n.-180-6581G>C