Canonical Allele Identifier: CA362868898

Gene: DTNBP1

Linked Data

• MyVariant Identifiers: chr6:g.15627607T>A (hg19) ; chr6:g.15627376T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15627376T>A , CM000668.2:g.15627376T>A	GRCh38
NC_000006.11:g.15627607T>A , CM000668.1:g.15627607T>A	GRCh37
NC_000006.10:g.15735586T>A	NCBI36
NG_009309.1:g.40665A>T , LRG_588:g.40665A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344537.10:c.322A>T MANE Select	ENSP00000341680.6:p.Ile108Phe
ENST00000338950.9:c.322A>T	ENSP00000344718.5:p.Ile108Phe
ENST00000344537.9:c.322A>T	ENSP00000341680.5:p.Ile108Phe
ENST00000355917.7:c.271A>T	ENSP00000348183.4:p.Ile91Phe
ENST00000506844.1:c.*320A>T	ENSP00000424202.1:n.*320A>T
ENST00000510395.5:c.*232A>T	ENSP00000424685.1:n.*232A>T
ENST00000511762.2:c.217A>T	ENSP00000427473.2:p.Ile73Phe
ENST00000513680.5:c.*320A>T	ENSP00000424357.1:n.*320A>T
ENST00000515875.5:c.271A>T	ENSP00000425495.1:p.Ile91Phe
ENST00000622898.4:c.217A>T	ENSP00000481997.1:p.Ile73Phe
NM_001271667.1:c.79A>T	NP_001258596.1:p.Ile27Phe
NM_001271668.1:c.271A>T	NP_001258597.1:p.Ile91Phe
NM_001271669.1:c.217A>T	NP_001258598.1:p.Ile73Phe
NM_032122.4:c.322A>T , LRG_588t1:c.322A>T	NP_115498.2:p.Ile108Phe
NM_183040.2:c.322A>T , LRG_588t2:c.322A>T	NP_898861.1:p.Ile108Phe
NR_036448.1:n.650A>T
XM_005249447.3:c.283A>T	XP_005249504.1:p.Ile95Phe
XM_011514936.1:c.232A>T	XP_011513238.1:p.Ile78Phe
XM_005249447.4:c.283A>T	XP_005249504.1:p.Ile95Phe
XM_011514936.3:c.232A>T	XP_011513238.1:p.Ile78Phe
NM_032122.5:c.322A>T MANE Select	NP_115498.2:p.Ile108Phe
NR_036448.2:n.620A>T
NM_001271667.2:c.79A>T	NP_001258596.1:p.Ile27Phe
NM_001271668.2:c.271A>T	NP_001258597.1:p.Ile91Phe
NM_001271669.2:c.217A>T	NP_001258598.1:p.Ile73Phe
NR_036448.3:n.620A>T