Canonical Allele Identifier: CA1753256991

Gene: XRCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152660562A= , CM000669.2:g.152660562A=	GRCh38
NC_000007.13:g.152357647A= , CM000669.1:g.152357647A=	GRCh37
NC_000007.12:g.151988580A=	NCBI36
NG_027988.1:g.20604T=
NG_027988.2:g.20604T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000698506.1:c.-47-11199T=	ENSP00000513758.1:n.-47-11199T=
ENST00000698507.1:n.328T=
ENST00000359321.2:c.121+139T= MANE Select	ENSP00000352271.1:n.121+139T=
ENST00000359321.1:c.121+139T=	ENSP00000352271.1:n.121+139T=
ENST00000495707.1:n.143+139T=
NM_005431.1:c.121+139T=	NP_005422.1:n.121+139T=
NM_005431.2:c.121+139T= MANE Select	NP_005422.1:n.121+139T=