Canonical Allele Identifier: CA1603608738

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177404015T= , CM000667.2:g.177404015T= GRCh38
NC_000005.9:g.176831016T= , CM000667.1:g.176831016T= GRCh37
NC_000005.8:g.176763622T= NCBI36
NG_007568.1:g.10562A= , LRG_145:g.10562A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696192.1:c.*760A= (F12) ENSP00000512476.1:n.*760A=
ENST00000696193.1:c.*1481A= (F12) ENSP00000512477.1:n.*1481A=
ENST00000696194.1:c.*684A= (F12) ENSP00000512478.1:n.*684A=
ENST00000696195.1:n.3897A= (F12)
ENST00000696200.1:n.1197A= (F12)
ENST00000696201.1:c.1094A= (F12) ENSP00000512482.1:p.Lys365=
ENST00000253496.4:c.1094A= (F12) MANE Select ENSP00000253496.3:p.Lys365=
ENST00000253496.3:c.1094A= (F12) ENSP00000253496.3:p.Lys365=
ENST00000502598.5:c.-45+489T= (GRK6) ENSP00000422873.1:n.-45+489T=
ENST00000502854.5:n.353A= (F12)
ENST00000503736.1:n.466A= (F12)
ENST00000510358.5:n.458A= (F12)
NM_000505.3:c.1094A= , LRG_145t1:c.1094A= (F12) NP_000496.2:p.Lys365=
XM_011534461.1:c.1094A= (F12) XP_011532763.1:p.Lys365=
XM_011534462.1:c.758A= (F12) XP_011532764.1:p.Lys253=
XM_011534462.2:c.758A= (F12) XP_011532764.1:p.Lys253=
XM_017009773.2:c.1416+6941T= (SLC34A1) XP_016865262.1:n.1416+6941T=
NM_000505.4:c.1094A= (F12) MANE Select NP_000496.2:p.Lys365=