Canonical Allele Identifier: CA362869112

Gene: DTNBP1

Linked Data

• MyVariant Identifiers: chr6:g.15627702A>T (hg19) ; chr6:g.15627471A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15627471A>T , CM000668.2:g.15627471A>T	GRCh38
NC_000006.11:g.15627702A>T , CM000668.1:g.15627702A>T	GRCh37
NC_000006.10:g.15735681A>T	NCBI36
NG_009309.1:g.40570T>A , LRG_588:g.40570T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344537.10:c.227T>A MANE Select	ENSP00000341680.6:p.Val76Glu
ENST00000338950.9:c.227T>A	ENSP00000344718.5:p.Val76Glu
ENST00000344537.9:c.227T>A	ENSP00000341680.5:p.Val76Glu
ENST00000355917.7:c.176T>A	ENSP00000348183.4:p.Val59Glu
ENST00000506844.1:c.*225T>A	ENSP00000424202.1:n.*225T>A
ENST00000510395.5:c.*137T>A	ENSP00000424685.1:n.*137T>A
ENST00000511762.2:c.122T>A	ENSP00000427473.2:p.Val41Glu
ENST00000513680.5:c.*225T>A	ENSP00000424357.1:n.*225T>A
ENST00000515875.5:c.176T>A	ENSP00000425495.1:p.Val59Glu
ENST00000622898.4:c.122T>A	ENSP00000481997.1:p.Val41Glu
NM_001271667.1:c.-17T>A	NP_001258596.1:n.-17T>A
NM_001271668.1:c.176T>A	NP_001258597.1:p.Val59Glu
NM_001271669.1:c.122T>A	NP_001258598.1:p.Val41Glu
NM_032122.4:c.227T>A , LRG_588t1:c.227T>A	NP_115498.2:p.Val76Glu
NM_183040.2:c.227T>A , LRG_588t2:c.227T>A	NP_898861.1:p.Val76Glu
NR_036448.1:n.555T>A
XM_005249447.3:c.188T>A	XP_005249504.1:p.Val63Glu
XM_011514936.1:c.137T>A	XP_011513238.1:p.Val46Glu
XM_005249447.4:c.188T>A	XP_005249504.1:p.Val63Glu
XM_011514936.3:c.137T>A	XP_011513238.1:p.Val46Glu
NM_032122.5:c.227T>A MANE Select	NP_115498.2:p.Val76Glu
NR_036448.2:n.525T>A
NM_001271667.2:c.-17T>A	NP_001258596.1:n.-17T>A
NM_001271668.2:c.176T>A	NP_001258597.1:p.Val59Glu
NM_001271669.2:c.122T>A	NP_001258598.1:p.Val41Glu
NR_036448.3:n.525T>A