Canonical Allele Identifier: CA448827271

Gene: DTNBP1

Linked Data

• gnomAD v4: 6-15627443-C-G
• MyVariant Identifiers: chr6:g.15627674C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15627443C>G , CM000668.2:g.15627443C>G	GRCh38
NC_000006.11:g.15627674C>G , CM000668.1:g.15627674C>G	GRCh37
NC_000006.10:g.15735653C>G	NCBI36
NG_009309.1:g.40598G>C , LRG_588:g.40598G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344537.10:c.255G>C MANE Select	ENSP00000341680.6:p.Ala85=
ENST00000338950.9:c.255G>C	ENSP00000344718.5:p.Ala85=
ENST00000344537.9:c.255G>C	ENSP00000341680.5:p.Ala85=
ENST00000355917.7:c.204G>C	ENSP00000348183.4:p.Ala68=
ENST00000506844.1:c.*253G>C	ENSP00000424202.1:n.*253G>C
ENST00000510395.5:c.*165G>C	ENSP00000424685.1:n.*165G>C
ENST00000511762.2:c.150G>C	ENSP00000427473.2:p.Ala50=
ENST00000513680.5:c.*253G>C	ENSP00000424357.1:n.*253G>C
ENST00000515875.5:c.204G>C	ENSP00000425495.1:p.Ala68=
ENST00000622898.4:c.150G>C	ENSP00000481997.1:p.Ala50=
NM_001271667.1:c.12G>C	NP_001258596.1:p.Ala4=
NM_001271668.1:c.204G>C	NP_001258597.1:p.Ala68=
NM_001271669.1:c.150G>C	NP_001258598.1:p.Ala50=
NM_032122.4:c.255G>C , LRG_588t1:c.255G>C	NP_115498.2:p.Ala85=
NM_183040.2:c.255G>C , LRG_588t2:c.255G>C	NP_898861.1:p.Ala85=
NR_036448.1:n.583G>C
XM_005249447.3:c.216G>C	XP_005249504.1:p.Ala72=
XM_011514936.1:c.165G>C	XP_011513238.1:p.Ala55=
XM_005249447.4:c.216G>C	XP_005249504.1:p.Ala72=
XM_011514936.3:c.165G>C	XP_011513238.1:p.Ala55=
NM_032122.5:c.255G>C MANE Select	NP_115498.2:p.Ala85=
NR_036448.2:n.553G>C
NM_001271667.2:c.12G>C	NP_001258596.1:p.Ala4=
NM_001271668.2:c.204G>C	NP_001258597.1:p.Ala68=
NM_001271669.2:c.150G>C	NP_001258598.1:p.Ala50=
NR_036448.3:n.553G>C