Canonical Allele Identifier: CA1657068778
Gene: FRK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.116065971C= , CM000668.2:g.116065971C= GRCh38
NC_000006.11:g.116387134C= , CM000668.1:g.116387134C= GRCh37
NC_000006.10:g.116493827C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_005266882.3:c.-283-5377G= XP_005266939.1:n.-283-5377G=
XM_011535653.1:c.-286-5374G= XP_011533955.1:n.-286-5374G=
XM_011535654.1:c.-286-5374G= XP_011533956.1:n.-286-5374G=
XM_011535655.1:c.-283-5377G= XP_011533957.1:n.-283-5377G=
XM_011535656.1:c.5+34521G= XP_011533958.1:n.5+34521G=
XM_005266882.4:c.-283-5377G= XP_005266939.1:n.-283-5377G=
XM_011535653.2:c.-286-5374G= XP_011533955.1:n.-286-5374G=
XM_011535654.2:c.-286-5374G= XP_011533956.1:n.-286-5374G=
XM_011535655.2:c.-283-5377G= XP_011533957.1:n.-283-5377G=
XM_011535656.2:c.5+34521G= XP_011533958.1:n.5+34521G=