Canonical Allele Identifier: CA1583226780

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132579223T= , CM000667.2:g.132579223T=	GRCh38
NC_000005.9:g.131914915T= , CM000667.1:g.131914915T=	GRCh37
NC_000005.8:g.131942814T=	NCBI36
NG_021151.1:g.27300T=
NG_021151.2:g.27247T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.366-94T= MANE Select	ENSP00000368100.4:n.366-94T=
ENST00000638452.2:c.69-94T=	ENSP00000492349.2:n.69-94T=
ENST00000638504.1:n.442+3295T=
ENST00000638568.2:c.69-94T=	ENSP00000491158.2:n.69-94T=
ENST00000639899.1:n.526-94T=
ENST00000640655.2:c.69-94T=	ENSP00000491596.2:n.69-94T=
ENST00000651160.1:c.366-94T=	ENSP00000498829.1:n.366-94T=
ENST00000651541.1:c.69-94T=	ENSP00000498795.1:n.69-94T=
ENST00000651658.1:n.434-94T=
ENST00000651723.1:c.*449-94T=	ENSP00000498237.1:n.*449-94T=
ENST00000652016.1:c.366-94T=	ENSP00000498267.1:n.366-94T=
ENST00000652485.1:c.366-94T=	ENSP00000498973.1:n.366-94T=
ENST00000378823.7:c.366-94T=	ENSP00000368100.4:n.366-94T=
ENST00000416135.5:c.69-94T=	ENSP00000389515.1:n.69-94T=
ENST00000423956.5:c.366-94T=	ENSP00000390971.1:n.366-94T=
ENST00000453394.5:c.366-94T=	ENSP00000400049.1:n.366-94T=
ENST00000533482.5:c.301-94T=	ENSP00000431225.1:n.301-94T=
NM_005732.3:c.366-94T=	NP_005723.2:n.366-94T=
NM_005732.4:c.366-94T= MANE Select	NP_005723.2:n.366-94T=