Canonical Allele Identifier: CA741748969

Gene: DSTN

Linked Data

• dbSNP Id: rs1362325882
• gnomAD v3: 20-17585347-G-A
• gnomAD v4: 20-17585347-G-A
• MyVariant Identifiers: chr20:g.17565992G>A (hg19) ; chr20:g.17585347G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.17585347G>A , CM000682.2:g.17585347G>A	GRCh38
NC_000020.10:g.17565992G>A , CM000682.1:g.17565992G>A	GRCh37
NC_000020.9:g.17513992G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000246069.12:c.3+15136G>A MANE Select	ENSP00000246069.6:n.3+15136G>A
ENST00000246069.11:c.3+15136G>A	ENSP00000246069.6:n.3+15136G>A
ENST00000449141.2:c.3+15136G>A	ENSP00000434355.1:n.3+15136G>A
ENST00000474024.5:c.-180-6585G>A	ENSP00000476975.1:n.-180-6585G>A
NM_001011546.1:c.-180-6585G>A	NP_001011546.1:n.-180-6585G>A
NM_006870.3:c.3+15136G>A	NP_006861.1:n.3+15136G>A
XM_011529142.1:c.3+15136G>A	XP_011527444.1:n.3+15136G>A
XM_011529143.1:c.3+15136G>A	XP_011527445.1:n.3+15136G>A
XM_011529144.1:c.-180-6585G>A	XP_011527446.1:n.-180-6585G>A
NM_006870.4:c.3+15136G>A MANE Select	NP_006861.1:n.3+15136G>A
NM_001011546.2:c.-180-6585G>A	NP_001011546.1:n.-180-6585G>A