Canonical Allele Identifier: CA15747489

Gene: RNF10

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120536707C>T , CM000674.2:g.120536707C>T	GRCh38
NC_000012.11:g.120974510C>T , CM000674.1:g.120974510C>T	GRCh37
NC_000012.10:g.119458893C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_014868.5:c.157+1739C>T MANE Select	NP_055683.3:n.157+1739C>T
ENST00000325954.9:c.157+1739C>T MANE Select	ENSP00000322242.4:n.157+1739C>T
NM_001330474.1:c.157+1739C>T	NP_001317403.1:n.157+1739C>T
NM_001330474.2:c.157+1739C>T	NP_001317403.1:n.157+1739C>T
NM_014868.4:c.157+1739C>T	NP_055683.3:n.157+1739C>T
ENST00000325954.8:c.157+1739C>T	ENSP00000322242.4:n.157+1739C>T
ENST00000413266.6:c.157+1739C>T	ENSP00000415682.2:n.157+1739C>T
ENST00000536869.5:c.97+1739C>T	ENSP00000443790.1:n.97+1739C>T
ENST00000537997.1:c.-95+1165C>T	ENSP00000443235.1:n.-95+1165C>T
ENST00000538796.5:c.157+1739C>T	ENSP00000443000.1:n.157+1739C>T
ENST00000542438.1:c.157+1739C>T	ENSP00000444770.1:n.157+1739C>T
ENST00000551139.6:n.115+1739C>T
XM_005254013.1:c.-95+1739C>T	XP_005254070.1:n.-95+1739C>T
XM_005254013.2:c.-95+1739C>T	XP_005254070.1:n.-95+1739C>T
XM_005254014.2:c.157+1739C>T	XP_005254071.1:n.157+1739C>T
XM_006719717.1:c.157+1739C>T	XP_006719780.1:n.157+1739C>T
XM_017020282.1:c.-95+1739C>T	XP_016875771.1:n.-95+1739C>T
XM_017020283.2:c.157+1739C>T	XP_016875772.1:n.157+1739C>T
XR_001748933.2:n.616+1739C>T
XR_001748934.2:n.616+1739C>T
XR_001748935.2:n.616+1739C>T
XR_001748936.2:n.616+1739C>T
XR_001748937.2:n.616+1739C>T
XR_001748938.2:n.616+1739C>T
XR_001748939.1:n.616+1739C>T
XR_243026.2:n.661+1739C>T
XR_243026.4:n.616+1739C>T
XR_429123.1:n.661+1739C>T
XR_944849.1:n.661+1739C>T
XR_944849.3:n.616+1739C>T
XR_944850.1:n.661+1739C>T