Canonical Allele Identifier: CA448827998

Gene: DTNBP1

Linked Data

• MyVariant Identifiers: chr6:g.15637987T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15637756T>G , CM000668.2:g.15637756T>G	GRCh38
NC_000006.11:g.15637987T>G , CM000668.1:g.15637987T>G	GRCh37
NC_000006.10:g.15745966T>G	NCBI36
NG_009309.1:g.30285A>C , LRG_588:g.30285A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344537.10:c.210A>C MANE Select	ENSP00000341680.6:p.Ala70=
ENST00000338950.9:c.210A>C	ENSP00000344718.5:p.Ala70=
ENST00000344537.9:c.210A>C	ENSP00000341680.5:p.Ala70=
ENST00000355917.7:c.159A>C	ENSP00000348183.4:p.Ala53=
ENST00000506844.1:c.*208A>C	ENSP00000424202.1:n.*208A>C
ENST00000510395.5:c.*120A>C	ENSP00000424685.1:n.*120A>C
ENST00000511762.2:c.105A>C	ENSP00000427473.2:p.Ala35=
ENST00000513680.5:c.*208A>C	ENSP00000424357.1:n.*208A>C
ENST00000515875.5:c.159A>C	ENSP00000425495.1:p.Ala53=
ENST00000622898.4:c.105A>C	ENSP00000481997.1:p.Ala35=
NM_001271667.1:c.-34A>C	NP_001258596.1:n.-34A>C
NM_001271668.1:c.159A>C	NP_001258597.1:p.Ala53=
NM_001271669.1:c.105A>C	NP_001258598.1:p.Ala35=
NM_032122.4:c.210A>C , LRG_588t1:c.210A>C	NP_115498.2:p.Ala70=
NM_183040.2:c.210A>C , LRG_588t2:c.210A>C	NP_898861.1:p.Ala70=
NR_036448.1:n.538A>C
XM_005249447.3:c.171A>C	XP_005249504.1:p.Ala57=
XM_011514936.1:c.120A>C	XP_011513238.1:p.Ala40=
XM_005249447.4:c.171A>C	XP_005249504.1:p.Ala57=
XM_011514936.3:c.120A>C	XP_011513238.1:p.Ala40=
NM_032122.5:c.210A>C MANE Select	NP_115498.2:p.Ala70=
NR_036448.2:n.508A>C
NM_001271667.2:c.-34A>C	NP_001258596.1:n.-34A>C
NM_001271668.2:c.159A>C	NP_001258597.1:p.Ala53=
NM_001271669.2:c.105A>C	NP_001258598.1:p.Ala35=
NR_036448.3:n.508A>C