Canonical Allele Identifier: CA351537879

Gene: XPC

Linked Data

• MyVariant Identifiers: chr3:g.14190175A>C (hg19) ; chr3:g.14148675A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14148675A>C , CM000665.2:g.14148675A>C	GRCh38
NC_000003.11:g.14190175A>C , CM000665.1:g.14190175A>C	GRCh37
NC_000003.10:g.14165176A>C	NCBI36
NG_011763.1:g.34998T>G , LRG_472:g.34998T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285021.12:c.2307T>G MANE Select	ENSP00000285021.8:p.Ile769Met
ENST00000285021.11:c.2307T>G	ENSP00000285021.7:p.Ile769Met
ENST00000427795.2:n.172T>G
ENST00000476581.6:c.*1760T>G	ENSP00000424548.1:n.*1760T>G
NM_004628.4:c.2307T>G , LRG_472t1:c.2307T>G	NP_004619.3:p.Ile769Met
NR_027299.1:n.2287T>G
XM_011534092.1:c.2307T>G	XP_011532394.1:p.Ile769Met
NM_001354726.1:c.1728T>G	NP_001341655.1:p.Ile576Met
NM_001354727.1:c.2301T>G	NP_001341656.1:p.Ile767Met
NM_001354729.1:c.2289T>G	NP_001341658.1:p.Ile763Met
NM_001354730.1:c.2061T>G	NP_001341659.1:p.Ile687Met
NR_148950.1:n.2250T>G
NR_148951.1:n.2126T>G
XR_001740256.2:n.2340T>G
XR_002959580.1:n.2340T>G
XR_002959581.1:n.3957T>G
NM_001354727.2:c.2301T>G	NP_001341656.1:p.Ile767Met
NM_004628.5:c.2307T>G MANE Select	NP_004619.3:p.Ile769Met
NR_148950.2:n.2179T>G
NR_148951.2:n.2055T>G
NM_001354726.2:c.1728T>G	NP_001341655.1:p.Ile576Met
NM_001354729.2:c.2289T>G	NP_001341658.1:p.Ile763Met
NM_001354730.2:c.2061T>G	NP_001341659.1:p.Ile687Met