Canonical Allele Identifier: CA362868855

Gene: DTNBP1

Linked Data

• MyVariant Identifiers: chr6:g.15627587C>G (hg19) ; chr6:g.15627356C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15627356C>G , CM000668.2:g.15627356C>G	GRCh38
NC_000006.11:g.15627587C>G , CM000668.1:g.15627587C>G	GRCh37
NC_000006.10:g.15735566C>G	NCBI36
NG_009309.1:g.40685G>C , LRG_588:g.40685G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344537.10:c.342G>C MANE Select	ENSP00000341680.6:p.Met114Ile
ENST00000338950.9:c.342G>C	ENSP00000344718.5:p.Met114Ile
ENST00000344537.9:c.342G>C	ENSP00000341680.5:p.Met114Ile
ENST00000355917.7:c.291G>C	ENSP00000348183.4:p.Met97Ile
ENST00000506844.1:c.*340G>C	ENSP00000424202.1:n.*340G>C
ENST00000510395.5:c.*252G>C	ENSP00000424685.1:n.*252G>C
ENST00000511762.2:c.237G>C	ENSP00000427473.2:p.Met79Ile
ENST00000513680.5:c.*340G>C	ENSP00000424357.1:n.*340G>C
ENST00000515875.5:c.291G>C	ENSP00000425495.1:p.Met97Ile
ENST00000622898.4:c.237G>C	ENSP00000481997.1:p.Met79Ile
NM_001271667.1:c.99G>C	NP_001258596.1:p.Met33Ile
NM_001271668.1:c.291G>C	NP_001258597.1:p.Met97Ile
NM_001271669.1:c.237G>C	NP_001258598.1:p.Met79Ile
NM_032122.4:c.342G>C , LRG_588t1:c.342G>C	NP_115498.2:p.Met114Ile
NM_183040.2:c.342G>C , LRG_588t2:c.342G>C	NP_898861.1:p.Met114Ile
NR_036448.1:n.670G>C
XM_005249447.3:c.303G>C	XP_005249504.1:p.Met101Ile
XM_011514936.1:c.252G>C	XP_011513238.1:p.Met84Ile
XM_005249447.4:c.303G>C	XP_005249504.1:p.Met101Ile
XM_011514936.3:c.252G>C	XP_011513238.1:p.Met84Ile
NM_032122.5:c.342G>C MANE Select	NP_115498.2:p.Met114Ile
NR_036448.2:n.640G>C
NM_001271667.2:c.99G>C	NP_001258596.1:p.Met33Ile
NM_001271668.2:c.291G>C	NP_001258597.1:p.Met97Ile
NM_001271669.2:c.237G>C	NP_001258598.1:p.Met79Ile
NR_036448.3:n.640G>C