Canonical Allele Identifier: CA362869047

Gene: DTNBP1

Linked Data

• dbSNP Id: rs1390984875
• MyVariant Identifiers: chr6:g.15627673G>C (hg19) ; chr6:g.15627442G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15627442G>C , CM000668.2:g.15627442G>C	GRCh38
NC_000006.11:g.15627673G>C , CM000668.1:g.15627673G>C	GRCh37
NC_000006.10:g.15735652G>C	NCBI36
NG_009309.1:g.40599C>G , LRG_588:g.40599C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344537.10:c.256C>G MANE Select	ENSP00000341680.6:p.His86Asp
ENST00000338950.9:c.256C>G	ENSP00000344718.5:p.His86Asp
ENST00000344537.9:c.256C>G	ENSP00000341680.5:p.His86Asp
ENST00000355917.7:c.205C>G	ENSP00000348183.4:p.His69Asp
ENST00000506844.1:c.*254C>G	ENSP00000424202.1:n.*254C>G
ENST00000510395.5:c.*166C>G	ENSP00000424685.1:n.*166C>G
ENST00000511762.2:c.151C>G	ENSP00000427473.2:p.His51Asp
ENST00000513680.5:c.*254C>G	ENSP00000424357.1:n.*254C>G
ENST00000515875.5:c.205C>G	ENSP00000425495.1:p.His69Asp
ENST00000622898.4:c.151C>G	ENSP00000481997.1:p.His51Asp
NM_001271667.1:c.13C>G	NP_001258596.1:p.His5Asp
NM_001271668.1:c.205C>G	NP_001258597.1:p.His69Asp
NM_001271669.1:c.151C>G	NP_001258598.1:p.His51Asp
NM_032122.4:c.256C>G , LRG_588t1:c.256C>G	NP_115498.2:p.His86Asp
NM_183040.2:c.256C>G , LRG_588t2:c.256C>G	NP_898861.1:p.His86Asp
NR_036448.1:n.584C>G
XM_005249447.3:c.217C>G	XP_005249504.1:p.His73Asp
XM_011514936.1:c.166C>G	XP_011513238.1:p.His56Asp
XM_005249447.4:c.217C>G	XP_005249504.1:p.His73Asp
XM_011514936.3:c.166C>G	XP_011513238.1:p.His56Asp
NM_032122.5:c.256C>G MANE Select	NP_115498.2:p.His86Asp
NR_036448.2:n.554C>G
NM_001271667.2:c.13C>G	NP_001258596.1:p.His5Asp
NM_001271668.2:c.205C>G	NP_001258597.1:p.His69Asp
NM_001271669.2:c.151C>G	NP_001258598.1:p.His51Asp
NR_036448.3:n.554C>G