Canonical Allele Identifier: CA821260653

Gene: DTNBP1

Linked Data

• dbSNP Id: rs1337455627
• gnomAD v3: 6-15650935-T-C
• gnomAD v4: 6-15650935-T-C
• MyVariant Identifiers: chr6:g.15651166T>C (hg19) ; chr6:g.15650935T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15650935T>C , CM000668.2:g.15650935T>C	GRCh38
NC_000006.11:g.15651166T>C , CM000668.1:g.15651166T>C	GRCh37
NC_000006.10:g.15759145T>C	NCBI36
NG_009309.1:g.17106A>G , LRG_588:g.17106A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000344537.10:c.161+378A>G MANE Select	ENSP00000341680.6:n.161+378A>G
ENST00000338950.9:c.161+378A>G	ENSP00000344718.5:n.161+378A>G
ENST00000344537.9:c.161+378A>G	ENSP00000341680.5:n.161+378A>G
ENST00000355917.7:c.110+1152A>G	ENSP00000348183.4:n.110+1152A>G
ENST00000506844.1:c.*159+378A>G	ENSP00000424202.1:n.*159+378A>G
ENST00000510395.5:c.*71+378A>G	ENSP00000424685.1:n.*71+378A>G
ENST00000511762.2:c.56+11879A>G	ENSP00000427473.2:n.56+11879A>G
ENST00000513680.5:c.*159+378A>G	ENSP00000424357.1:n.*159+378A>G
ENST00000515875.5:c.110+1152A>G	ENSP00000425495.1:n.110+1152A>G
ENST00000622898.4:c.56+11879A>G	ENSP00000481997.1:n.56+11879A>G
NM_001271667.1:c.-83+378A>G	NP_001258596.1:n.-83+378A>G
NM_001271668.1:c.110+1152A>G	NP_001258597.1:n.110+1152A>G
NM_001271669.1:c.56+11879A>G	NP_001258598.1:n.56+11879A>G
NM_032122.4:c.161+378A>G , LRG_588t1:c.161+378A>G	NP_115498.2:n.161+378A>G
NM_183040.2:c.161+378A>G , LRG_588t2:c.161+378A>G	NP_898861.1:n.161+378A>G
NR_036448.1:n.489+378A>G
XM_005249447.3:c.122+378A>G	XP_005249504.1:n.122+378A>G
XM_011514936.1:c.71+1152A>G	XP_011513238.1:n.71+1152A>G
XM_005249447.4:c.122+378A>G	XP_005249504.1:n.122+378A>G
XM_011514936.3:c.71+1152A>G	XP_011513238.1:n.71+1152A>G
NM_032122.5:c.161+378A>G MANE Select	NP_115498.2:n.161+378A>G
NR_036448.2:n.459+378A>G
NM_001271667.2:c.-83+378A>G	NP_001258596.1:n.-83+378A>G
NM_001271668.2:c.110+1152A>G	NP_001258597.1:n.110+1152A>G
NM_001271669.2:c.56+11879A>G	NP_001258598.1:n.56+11879A>G
NR_036448.3:n.459+378A>G