Canonical Allele Identifier: CA2353123703

Gene: DSTN

Linked Data

• dbSNP Id: rs2035394301

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.17585425_17585428del , CM000682.2:g.17585425_17585428del	GRCh38
NC_000020.10:g.17566070_17566073del , CM000682.1:g.17566070_17566073del	GRCh37
NC_000020.9:g.17514070_17514073del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000246069.12:c.3+15214_3+15217del MANE Select	ENSP00000246069.6:n.3+15214_3+15217del
ENST00000246069.11:c.3+15214_3+15217del	ENSP00000246069.6:n.3+15214_3+15217del
ENST00000449141.2:c.3+15214_3+15217del	ENSP00000434355.1:n.3+15214_3+15217del
ENST00000474024.5:c.-180-6507_-180-6504del	ENSP00000476975.1:n.-180-6507_-180-6504de...
NM_001011546.1:c.-180-6507_-180-6504del	NP_001011546.1:n.-180-6507_-180-6504del
NM_006870.3:c.3+15214_3+15217del	NP_006861.1:n.3+15214_3+15217del
XM_011529142.1:c.3+15214_3+15217del	XP_011527444.1:n.3+15214_3+15217del
XM_011529143.1:c.3+15214_3+15217del	XP_011527445.1:n.3+15214_3+15217del
XM_011529144.1:c.-180-6507_-180-6504del	XP_011527446.1:n.-180-6507_-180-6504del
NM_006870.4:c.3+15214_3+15217del MANE Select	NP_006861.1:n.3+15214_3+15217del
NM_001011546.2:c.-180-6507_-180-6504del	NP_001011546.1:n.-180-6507_-180-6504del