Canonical Allele Identifier: CA804005507

Gene: RAD50

Linked Data

• dbSNP Id: rs1241171232
• MyVariant Identifiers: chr5:g.131892705A>C (hg19) ; chr5:g.132557013A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132557013A>C , CM000667.2:g.132557013A>C	GRCh38
NC_000005.9:g.131892705A>C , CM000667.1:g.131892705A>C	GRCh37
NC_000005.8:g.131920604A>C	NCBI36
NG_021151.1:g.5090A>C
NG_021151.2:g.5037A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.-312A>C MANE Select	ENSP00000368100.4:n.-312A>C
ENST00000638452.2:c.-168-2271A>C	ENSP00000492349.2:n.-168-2271A>C
ENST00000638504.1:n.207-2271A>C
ENST00000638568.2:c.-169+540A>C	ENSP00000491158.2:n.-169+540A>C
ENST00000639899.1:n.290-2271A>C
ENST00000640655.2:c.-168-2271A>C	ENSP00000491596.2:n.-168-2271A>C
ENST00000651160.1:c.-312A>C	ENSP00000498829.1:n.-312A>C
ENST00000651541.1:c.-169+4A>C	ENSP00000498795.1:n.-169+4A>C
ENST00000652016.1:c.-312A>C	ENSP00000498267.1:n.-312A>C
ENST00000652485.1:c.-312A>C	ENSP00000498973.1:n.-312A>C
ENST00000378823.7:c.-312A>C	ENSP00000368100.4:n.-312A>C
ENST00000416135.5:c.-169+540A>C	ENSP00000389515.1:n.-169+540A>C
ENST00000533482.5:c.-312A>C	ENSP00000431225.1:n.-312A>C
NM_005732.3:c.-312A>C	NP_005723.2:n.-312A>C
NM_005732.4:c.-312A>C MANE Select	NP_005723.2:n.-312A>C