Canonical Allele Identifier: CA362868909

Gene: DTNBP1

Linked Data

• MyVariant Identifiers: chr6:g.15627612G>C (hg19) ; chr6:g.15627381G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15627381G>C , CM000668.2:g.15627381G>C	GRCh38
NC_000006.11:g.15627612G>C , CM000668.1:g.15627612G>C	GRCh37
NC_000006.10:g.15735591G>C	NCBI36
NG_009309.1:g.40660C>G , LRG_588:g.40660C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344537.10:c.317C>G MANE Select	ENSP00000341680.6:p.Ala106Gly
ENST00000338950.9:c.317C>G	ENSP00000344718.5:p.Ala106Gly
ENST00000344537.9:c.317C>G	ENSP00000341680.5:p.Ala106Gly
ENST00000355917.7:c.266C>G	ENSP00000348183.4:p.Ala89Gly
ENST00000506844.1:c.*315C>G	ENSP00000424202.1:n.*315C>G
ENST00000510395.5:c.*227C>G	ENSP00000424685.1:n.*227C>G
ENST00000511762.2:c.212C>G	ENSP00000427473.2:p.Ala71Gly
ENST00000513680.5:c.*315C>G	ENSP00000424357.1:n.*315C>G
ENST00000515875.5:c.266C>G	ENSP00000425495.1:p.Ala89Gly
ENST00000622898.4:c.212C>G	ENSP00000481997.1:p.Ala71Gly
NM_001271667.1:c.74C>G	NP_001258596.1:p.Ala25Gly
NM_001271668.1:c.266C>G	NP_001258597.1:p.Ala89Gly
NM_001271669.1:c.212C>G	NP_001258598.1:p.Ala71Gly
NM_032122.4:c.317C>G , LRG_588t1:c.317C>G	NP_115498.2:p.Ala106Gly
NM_183040.2:c.317C>G , LRG_588t2:c.317C>G	NP_898861.1:p.Ala106Gly
NR_036448.1:n.645C>G
XM_005249447.3:c.278C>G	XP_005249504.1:p.Ala93Gly
XM_011514936.1:c.227C>G	XP_011513238.1:p.Ala76Gly
XM_005249447.4:c.278C>G	XP_005249504.1:p.Ala93Gly
XM_011514936.3:c.227C>G	XP_011513238.1:p.Ala76Gly
NM_032122.5:c.317C>G MANE Select	NP_115498.2:p.Ala106Gly
NR_036448.2:n.615C>G
NM_001271667.2:c.74C>G	NP_001258596.1:p.Ala25Gly
NM_001271668.2:c.266C>G	NP_001258597.1:p.Ala89Gly
NM_001271669.2:c.212C>G	NP_001258598.1:p.Ala71Gly
NR_036448.3:n.615C>G