Canonical Allele Identifier: CA1657082762
Gene: FRK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.116097961G= , CM000668.2:g.116097961G= GRCh38
NC_000006.11:g.116419124G= , CM000668.1:g.116419124G= GRCh37
NC_000006.10:g.116525817G= NCBI36
NG_021351.1:g.2126G=

Transcript Alleles

HGVS Amino-acid Change
XM_005266882.3:c.-502+2531C= XP_005266939.1:n.-502+2531C=
XM_011535653.1:c.-505+2531C= XP_011533955.1:n.-505+2531C=
XM_011535654.1:c.-287+2531C= XP_011533956.1:n.-287+2531C=
XM_011535655.1:c.-284+2531C= XP_011533957.1:n.-284+2531C=
XM_011535656.1:c.5+2531C= XP_011533958.1:n.5+2531C=
XM_005266882.4:c.-502+2531C= XP_005266939.1:n.-502+2531C=
XM_011535653.2:c.-505+2531C= XP_011533955.1:n.-505+2531C=
XM_011535654.2:c.-287+2531C= XP_011533956.1:n.-287+2531C=
XM_011535655.2:c.-284+2531C= XP_011533957.1:n.-284+2531C=
XM_011535656.2:c.5+2531C= XP_011533958.1:n.5+2531C=