Canonical Allele Identifier: CA2830538729

Gene: RAD17

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.69385810C>A , CM000667.2:g.69385810C>A	GRCh38
NC_000005.9:g.68681637C>A , CM000667.1:g.68681637C>A	GRCh37
NC_000005.8:g.68717393C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354868.10:c.646-233C>A MANE Select	ENSP00000346938.5:n.646-233C>A
ENST00000282891.10:c.388-233C>A	ENSP00000282891.6:n.388-233C>A
ENST00000305138.8:c.646-233C>A	ENSP00000303134.4:n.646-233C>A
ENST00000345306.10:c.646-233C>A	ENSP00000311227.7:n.646-233C>A
ENST00000354312.7:c.646-233C>A	ENSP00000346271.3:n.646-233C>A
ENST00000354868.9:c.646-233C>A	ENSP00000346938.5:n.646-233C>A
ENST00000358030.6:c.151-233C>A	ENSP00000350725.2:n.151-233C>A
ENST00000361732.6:c.646-233C>A	ENSP00000355226.2:n.646-233C>A
ENST00000380774.7:c.679-233C>A	ENSP00000370151.3:n.679-233C>A
ENST00000504177.5:n.250+14639C>A
ENST00000509734.5:c.679-233C>A	ENSP00000426191.1:n.679-233C>A
ENST00000514626.1:n.256-233C>A
ENST00000521422.5:c.151-233C>A	ENSP00000427743.1:n.151-233C>A
ENST00000616683.4:c.646-233C>A	ENSP00000482775.1:n.646-233C>A
NM_001278622.1:c.646-233C>A	NP_001265551.1:n.646-233C>A
NM_002873.1:c.646-233C>A	NP_002864.1:n.646-233C>A
NM_133338.2:c.646-233C>A	NP_579916.1:n.646-233C>A
NM_133339.2:c.679-233C>A	NP_579917.1:n.679-233C>A
NM_133340.2:c.151-233C>A	NP_579918.1:n.151-233C>A
NM_133341.2:c.388-233C>A	NP_579919.1:n.388-233C>A
NM_133342.2:c.646-233C>A	NP_579920.1:n.646-233C>A
NM_133343.1:c.646-233C>A	NP_579921.1:n.646-233C>A
NM_133344.2:c.646-233C>A	NP_579922.1:n.646-233C>A
XM_017009681.1:c.646-233C>A	XP_016865170.1:n.646-233C>A
NM_133338.3:c.646-233C>A MANE Select	NP_579916.1:n.646-233C>A
NM_133342.3:c.646-233C>A	NP_579920.1:n.646-233C>A
NM_133344.3:c.646-233C>A	NP_579922.1:n.646-233C>A
NM_133343.2:c.646-233C>A	NP_579921.1:n.646-233C>A