Canonical Allele Identifier: CA2353123689

Gene: DSTN

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.17585363G= , CM000682.2:g.17585363G=	GRCh38
NC_000020.10:g.17566008G= , CM000682.1:g.17566008G=	GRCh37
NC_000020.9:g.17514008G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000246069.12:c.3+15152G= MANE Select	ENSP00000246069.6:n.3+15152G=
ENST00000246069.11:c.3+15152G=	ENSP00000246069.6:n.3+15152G=
ENST00000449141.2:c.3+15152G=	ENSP00000434355.1:n.3+15152G=
ENST00000474024.5:c.-180-6569G=	ENSP00000476975.1:n.-180-6569G=
NM_001011546.1:c.-180-6569G=	NP_001011546.1:n.-180-6569G=
NM_006870.3:c.3+15152G=	NP_006861.1:n.3+15152G=
XM_011529142.1:c.3+15152G=	XP_011527444.1:n.3+15152G=
XM_011529143.1:c.3+15152G=	XP_011527445.1:n.3+15152G=
XM_011529144.1:c.-180-6569G=	XP_011527446.1:n.-180-6569G=
NM_006870.4:c.3+15152G= MANE Select	NP_006861.1:n.3+15152G=
NM_001011546.2:c.-180-6569G=	NP_001011546.1:n.-180-6569G=