Canonical Allele Identifier: CA362868938

Gene: DTNBP1

Linked Data

• MyVariant Identifiers: chr6:g.15627625G>C (hg19) ; chr6:g.15627394G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15627394G>C , CM000668.2:g.15627394G>C	GRCh38
NC_000006.11:g.15627625G>C , CM000668.1:g.15627625G>C	GRCh37
NC_000006.10:g.15735604G>C	NCBI36
NG_009309.1:g.40647C>G , LRG_588:g.40647C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000344537.10:c.304C>G MANE Select	ENSP00000341680.6:p.Gln102Glu
ENST00000338950.9:c.304C>G	ENSP00000344718.5:p.Gln102Glu
ENST00000344537.9:c.304C>G	ENSP00000341680.5:p.Gln102Glu
ENST00000355917.7:c.253C>G	ENSP00000348183.4:p.Gln85Glu
ENST00000506844.1:c.*302C>G	ENSP00000424202.1:n.*302C>G
ENST00000510395.5:c.*214C>G	ENSP00000424685.1:n.*214C>G
ENST00000511762.2:c.199C>G	ENSP00000427473.2:p.Gln67Glu
ENST00000513680.5:c.*302C>G	ENSP00000424357.1:n.*302C>G
ENST00000515875.5:c.253C>G	ENSP00000425495.1:p.Gln85Glu
ENST00000622898.4:c.199C>G	ENSP00000481997.1:p.Gln67Glu
NM_001271667.1:c.61C>G	NP_001258596.1:p.Gln21Glu
NM_001271668.1:c.253C>G	NP_001258597.1:p.Gln85Glu
NM_001271669.1:c.199C>G	NP_001258598.1:p.Gln67Glu
NM_032122.4:c.304C>G , LRG_588t1:c.304C>G	NP_115498.2:p.Gln102Glu
NM_183040.2:c.304C>G , LRG_588t2:c.304C>G	NP_898861.1:p.Gln102Glu
NR_036448.1:n.632C>G
XM_005249447.3:c.265C>G	XP_005249504.1:p.Gln89Glu
XM_011514936.1:c.214C>G	XP_011513238.1:p.Gln72Glu
XM_005249447.4:c.265C>G	XP_005249504.1:p.Gln89Glu
XM_011514936.3:c.214C>G	XP_011513238.1:p.Gln72Glu
NM_032122.5:c.304C>G MANE Select	NP_115498.2:p.Gln102Glu
NR_036448.2:n.602C>G
NM_001271667.2:c.61C>G	NP_001258596.1:p.Gln21Glu
NM_001271668.2:c.253C>G	NP_001258597.1:p.Gln85Glu
NM_001271669.2:c.199C>G	NP_001258598.1:p.Gln67Glu
NR_036448.3:n.602C>G