Canonical Allele Identifier: CA362869618

Gene: DTNBP1

Linked Data

• MyVariant Identifiers: chr6:g.15638024G>C (hg19) ; chr6:g.15637793G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15637793G>C , CM000668.2:g.15637793G>C	GRCh38
NC_000006.11:g.15638024G>C , CM000668.1:g.15638024G>C	GRCh37
NC_000006.10:g.15746003G>C	NCBI36
NG_009309.1:g.30248C>G , LRG_588:g.30248C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000344537.10:c.173C>G MANE Select	ENSP00000341680.6:p.Thr58Arg
ENST00000338950.9:c.173C>G	ENSP00000344718.5:p.Thr58Arg
ENST00000344537.9:c.173C>G	ENSP00000341680.5:p.Thr58Arg
ENST00000355917.7:c.122C>G	ENSP00000348183.4:p.Thr41Arg
ENST00000506844.1:c.*171C>G	ENSP00000424202.1:n.*171C>G
ENST00000510395.5:c.*83C>G	ENSP00000424685.1:n.*83C>G
ENST00000511762.2:c.68C>G	ENSP00000427473.2:p.Thr23Arg
ENST00000513680.5:c.*171C>G	ENSP00000424357.1:n.*171C>G
ENST00000515875.5:c.122C>G	ENSP00000425495.1:p.Thr41Arg
ENST00000622898.4:c.68C>G	ENSP00000481997.1:p.Thr23Arg
NM_001271667.1:c.-71C>G	NP_001258596.1:n.-71C>G
NM_001271668.1:c.122C>G	NP_001258597.1:p.Thr41Arg
NM_001271669.1:c.68C>G	NP_001258598.1:p.Thr23Arg
NM_032122.4:c.173C>G , LRG_588t1:c.173C>G	NP_115498.2:p.Thr58Arg
NM_183040.2:c.173C>G , LRG_588t2:c.173C>G	NP_898861.1:p.Thr58Arg
NR_036448.1:n.501C>G
XM_005249447.3:c.134C>G	XP_005249504.1:p.Thr45Arg
XM_011514936.1:c.83C>G	XP_011513238.1:p.Thr28Arg
XM_005249447.4:c.134C>G	XP_005249504.1:p.Thr45Arg
XM_011514936.3:c.83C>G	XP_011513238.1:p.Thr28Arg
NM_032122.5:c.173C>G MANE Select	NP_115498.2:p.Thr58Arg
NR_036448.2:n.471C>G
NM_001271667.2:c.-71C>G	NP_001258596.1:n.-71C>G
NM_001271668.2:c.122C>G	NP_001258597.1:p.Thr41Arg
NM_001271669.2:c.68C>G	NP_001258598.1:p.Thr23Arg
NR_036448.3:n.471C>G