Canonical Allele Identifier: CA1603608770

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177404051C= , CM000667.2:g.177404051C= GRCh38
NC_000005.9:g.176831052C= , CM000667.1:g.176831052C= GRCh37
NC_000005.8:g.176763658C= NCBI36
NG_007568.1:g.10526G= , LRG_145:g.10526G=

Transcript Alleles

HGVS Amino-acid change
ENST00000696192.1:c.*724G= (F12) ENSP00000512476.1:n.*724G=
ENST00000696193.1:c.*1445G= (F12) ENSP00000512477.1:n.*1445G=
ENST00000696194.1:c.*648G= (F12) ENSP00000512478.1:n.*648G=
ENST00000696195.1:n.3861G= (F12)
ENST00000696200.1:n.1161G= (F12)
ENST00000696201.1:c.1058G= (F12) ENSP00000512482.1:p.Arg353=
ENST00000253496.4:c.1058G= (F12) MANE Select ENSP00000253496.3:p.Arg353=
ENST00000253496.3:c.1058G= (F12) ENSP00000253496.3:p.Arg353=
ENST00000502598.5:c.-45+525C= (GRK6) ENSP00000422873.1:n.-45+525C=
ENST00000502854.5:n.317G= (F12)
ENST00000503736.1:n.430G= (F12)
ENST00000510358.5:n.422G= (F12)
NM_000505.3:c.1058G= , LRG_145t1:c.1058G= (F12) NP_000496.2:p.Arg353=
XM_011534461.1:c.1058G= (F12) XP_011532763.1:p.Arg353=
XM_011534462.1:c.722G= (F12) XP_011532764.1:p.Arg241=
XM_011534462.2:c.722G= (F12) XP_011532764.1:p.Arg241=
XM_017009773.2:c.1416+6977C= (SLC34A1) XP_016865262.1:n.1416+6977C=
NM_000505.4:c.1058G= (F12) MANE Select NP_000496.2:p.Arg353=