Canonical Allele Identifier: CA448827217

Gene: DTNBP1

Linked Data

• MyVariant Identifiers: chr6:g.15627581T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15627350T>A , CM000668.2:g.15627350T>A	GRCh38
NC_000006.11:g.15627581T>A , CM000668.1:g.15627581T>A	GRCh37
NC_000006.10:g.15735560T>A	NCBI36
NG_009309.1:g.40691A>T , LRG_588:g.40691A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344537.10:c.348A>T MANE Select	ENSP00000341680.6:p.Ala116=
ENST00000338950.9:c.348A>T	ENSP00000344718.5:p.Ala116=
ENST00000344537.9:c.348A>T	ENSP00000341680.5:p.Ala116=
ENST00000355917.7:c.297A>T	ENSP00000348183.4:p.Ala99=
ENST00000506844.1:c.*346A>T	ENSP00000424202.1:n.*346A>T
ENST00000510395.5:c.*258A>T	ENSP00000424685.1:n.*258A>T
ENST00000511762.2:c.243A>T	ENSP00000427473.2:p.Ala81=
ENST00000513680.5:c.*346A>T	ENSP00000424357.1:n.*346A>T
ENST00000515875.5:c.297A>T	ENSP00000425495.1:p.Ala99=
ENST00000622898.4:c.243A>T	ENSP00000481997.1:p.Ala81=
NM_001271667.1:c.105A>T	NP_001258596.1:p.Ala35=
NM_001271668.1:c.297A>T	NP_001258597.1:p.Ala99=
NM_001271669.1:c.243A>T	NP_001258598.1:p.Ala81=
NM_032122.4:c.348A>T , LRG_588t1:c.348A>T	NP_115498.2:p.Ala116=
NM_183040.2:c.348A>T , LRG_588t2:c.348A>T	NP_898861.1:p.Ala116=
NR_036448.1:n.676A>T
XM_005249447.3:c.309A>T	XP_005249504.1:p.Ala103=
XM_011514936.1:c.258A>T	XP_011513238.1:p.Ala86=
XM_005249447.4:c.309A>T	XP_005249504.1:p.Ala103=
XM_011514936.3:c.258A>T	XP_011513238.1:p.Ala86=
NM_032122.5:c.348A>T MANE Select	NP_115498.2:p.Ala116=
NR_036448.2:n.646A>T
NM_001271667.2:c.105A>T	NP_001258596.1:p.Ala35=
NM_001271668.2:c.297A>T	NP_001258597.1:p.Ala99=
NM_001271669.2:c.243A>T	NP_001258598.1:p.Ala81=
NR_036448.3:n.646A>T