Canonical Allele Identifier: CA741749003

Gene: DSTN

Linked Data

• dbSNP Id: rs1454241960
• gnomAD v3: 20-17585491-T-C
• gnomAD v4: 20-17585491-T-C
• MyVariant Identifiers: chr20:g.17566136T>C (hg19) ; chr20:g.17585491T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.17585491T>C , CM000682.2:g.17585491T>C	GRCh38
NC_000020.10:g.17566136T>C , CM000682.1:g.17566136T>C	GRCh37
NC_000020.9:g.17514136T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246069.12:c.4-15247T>C MANE Select	ENSP00000246069.6:n.4-15247T>C
ENST00000246069.11:c.4-15247T>C	ENSP00000246069.6:n.4-15247T>C
ENST00000449141.2:c.4-15247T>C	ENSP00000434355.1:n.4-15247T>C
ENST00000474024.5:c.-180-6441T>C	ENSP00000476975.1:n.-180-6441T>C
NM_001011546.1:c.-180-6441T>C	NP_001011546.1:n.-180-6441T>C
NM_006870.3:c.4-15247T>C	NP_006861.1:n.4-15247T>C
XM_011529142.1:c.4-15247T>C	XP_011527444.1:n.4-15247T>C
XM_011529143.1:c.4-15247T>C	XP_011527445.1:n.4-15247T>C
XM_011529144.1:c.-180-6441T>C	XP_011527446.1:n.-180-6441T>C
NM_006870.4:c.4-15247T>C MANE Select	NP_006861.1:n.4-15247T>C
NM_001011546.2:c.-180-6441T>C	NP_001011546.1:n.-180-6441T>C