Canonical Allele Identifier: CA362869102

Gene: DTNBP1

Linked Data

• dbSNP Id: rs1238265151
• gnomAD v3: 6-15627467-A-C
• gnomAD v4: 6-15627467-A-C
• MyVariant Identifiers: chr6:g.15627698A>C (hg19) ; chr6:g.15627467A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15627467A>C , CM000668.2:g.15627467A>C	GRCh38
NC_000006.11:g.15627698A>C , CM000668.1:g.15627698A>C	GRCh37
NC_000006.10:g.15735677A>C	NCBI36
NG_009309.1:g.40574T>G , LRG_588:g.40574T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344537.10:c.231T>G MANE Select	ENSP00000341680.6:p.Asp77Glu
ENST00000338950.9:c.231T>G	ENSP00000344718.5:p.Asp77Glu
ENST00000344537.9:c.231T>G	ENSP00000341680.5:p.Asp77Glu
ENST00000355917.7:c.180T>G	ENSP00000348183.4:p.Asp60Glu
ENST00000506844.1:c.*229T>G	ENSP00000424202.1:n.*229T>G
ENST00000510395.5:c.*141T>G	ENSP00000424685.1:n.*141T>G
ENST00000511762.2:c.126T>G	ENSP00000427473.2:p.Asp42Glu
ENST00000513680.5:c.*229T>G	ENSP00000424357.1:n.*229T>G
ENST00000515875.5:c.180T>G	ENSP00000425495.1:p.Asp60Glu
ENST00000622898.4:c.126T>G	ENSP00000481997.1:p.Asp42Glu
NM_001271667.1:c.-13T>G	NP_001258596.1:n.-13T>G
NM_001271668.1:c.180T>G	NP_001258597.1:p.Asp60Glu
NM_001271669.1:c.126T>G	NP_001258598.1:p.Asp42Glu
NM_032122.4:c.231T>G , LRG_588t1:c.231T>G	NP_115498.2:p.Asp77Glu
NM_183040.2:c.231T>G , LRG_588t2:c.231T>G	NP_898861.1:p.Asp77Glu
NR_036448.1:n.559T>G
XM_005249447.3:c.192T>G	XP_005249504.1:p.Asp64Glu
XM_011514936.1:c.141T>G	XP_011513238.1:p.Asp47Glu
XM_005249447.4:c.192T>G	XP_005249504.1:p.Asp64Glu
XM_011514936.3:c.141T>G	XP_011513238.1:p.Asp47Glu
NM_032122.5:c.231T>G MANE Select	NP_115498.2:p.Asp77Glu
NR_036448.2:n.529T>G
NM_001271667.2:c.-13T>G	NP_001258596.1:n.-13T>G
NM_001271668.2:c.180T>G	NP_001258597.1:p.Asp60Glu
NM_001271669.2:c.126T>G	NP_001258598.1:p.Asp42Glu
NR_036448.3:n.529T>G