Canonical Allele Identifier: CA10634975

Gene: DCLRE1C

Linked Data

• ClinVar Variation Id: 299303
• ClinVar RCV Id: RCV000399569
• dbSNP Id: rs886046845
• gnomAD v3: 10-14908094-C-T
• gnomAD v4: 10-14908094-C-T
• MyVariant Identifiers: chr10:g.14950093C>T (hg19) ; chr10:g.14908094C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.14908094C>T , CM000672.2:g.14908094C>T	GRCh38
NC_000010.10:g.14950093C>T , CM000672.1:g.14950093C>T	GRCh37
NC_000010.9:g.14990099C>T	NCBI36
NG_007276.1:g.51002G>A , LRG_54:g.51002G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378241.6:c.*2581G>A	ENSP00000367487.3:n.*2581G>A
ENST00000456122.2:c.*1343-8782G>A	ENSP00000413180.3:n.*1343-8782G>A
ENST00000697047.1:c.1782+611G>A	ENSP00000513066.1:n.1782+611G>A
ENST00000697070.1:c.2029+364G>A	ENSP00000513085.1:n.2029+364G>A
ENST00000697071.1:c.*1702+611G>A	ENSP00000513086.1:n.*1702+611G>A
ENST00000697072.1:c.*794+611G>A	ENSP00000513087.1:n.*794+611G>A
ENST00000697073.1:c.*1560+611G>A	ENSP00000513088.2:n.*1560+611G>A
ENST00000697074.1:c.*1807+364G>A	ENSP00000513089.2:n.*1807+364G>A
ENST00000378278.7:c.*314G>A MANE Select	ENSP00000367527.2:n.*314G>A
ENST00000378246.6:c.*314G>A	ENSP00000367492.2:n.*314G>A
ENST00000378289.8:c.1157-8782G>A	ENSP00000367538.4:n.1157-8782G>A
NM_001033855.2:c.*314G>A	NP_001029027.1:n.*314G>A
NM_001033857.2:c.*314G>A	NP_001029029.1:n.*314G>A
NM_001033858.2:c.*314G>A	NP_001029030.1:n.*314G>A
NM_001289076.1:c.*314G>A	NP_001276005.1:n.*314G>A
NM_001289077.1:c.*314G>A	NP_001276006.1:n.*314G>A
NM_001289078.1:c.*314G>A	NP_001276007.1:n.*314G>A
NM_001289079.1:c.*314G>A	NP_001276008.1:n.*314G>A
NM_022487.3:c.*314G>A	NP_071932.2:n.*314G>A
NR_110297.1:n.3168G>A
NM_001350965.1:c.1782+611G>A	NP_001337894.1:n.1782+611G>A
NM_001350966.1:c.1437+611G>A	NP_001337895.1:n.1437+611G>A
NM_001350967.1:c.1422+611G>A	NP_001337896.1:n.1422+611G>A
NR_146960.1:n.2149+611G>A
NR_146961.1:n.2909G>A
NR_146962.1:n.2880G>A
XM_024448134.1:c.*314G>A	XP_024303902.1:n.*314G>A
XM_024448135.1:c.1437+611G>A	XP_024303903.1:n.1437+611G>A
NM_001033855.3:c.*314G>A MANE Select	NP_001029027.1:n.*314G>A
NM_001033857.3:c.*314G>A	NP_001029029.1:n.*314G>A
NM_001033858.3:c.*314G>A	NP_001029030.1:n.*314G>A
NM_001289076.2:c.*314G>A	NP_001276005.1:n.*314G>A
NM_001289077.2:c.*314G>A	NP_001276006.1:n.*314G>A
NM_001289078.2:c.*314G>A	NP_001276007.1:n.*314G>A
NM_001289079.2:c.*314G>A	NP_001276008.1:n.*314G>A
NM_001350965.2:c.1782+611G>A	NP_001337894.1:n.1782+611G>A
NM_001350966.2:c.1437+611G>A	NP_001337895.1:n.1437+611G>A
NM_001350967.2:c.1422+611G>A	NP_001337896.1:n.1422+611G>A
NM_022487.4:c.*314G>A	NP_071932.2:n.*314G>A
NR_110297.2:n.2832G>A
NR_146961.2:n.2573G>A