Canonical Allele Identifier: CA1603608762

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177404044G= , CM000667.2:g.177404044G= GRCh38
NC_000005.9:g.176831045G= , CM000667.1:g.176831045G= GRCh37
NC_000005.8:g.176763651G= NCBI36
NG_007568.1:g.10533C= , LRG_145:g.10533C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696192.1:c.*731C= (F12) ENSP00000512476.1:n.*731C=
ENST00000696193.1:c.*1452C= (F12) ENSP00000512477.1:n.*1452C=
ENST00000696194.1:c.*655C= (F12) ENSP00000512478.1:n.*655C=
ENST00000696195.1:n.3868C= (F12)
ENST00000696200.1:n.1168C= (F12)
ENST00000696201.1:c.1065C= (F12) ENSP00000512482.1:p.Gly355=
ENST00000253496.4:c.1065C= (F12) MANE Select ENSP00000253496.3:p.Gly355=
ENST00000253496.3:c.1065C= (F12) ENSP00000253496.3:p.Gly355=
ENST00000502598.5:c.-45+518G= (GRK6) ENSP00000422873.1:n.-45+518G=
ENST00000502854.5:n.324C= (F12)
ENST00000503736.1:n.437C= (F12)
ENST00000510358.5:n.429C= (F12)
NM_000505.3:c.1065C= , LRG_145t1:c.1065C= (F12) NP_000496.2:p.Gly355=
XM_011534461.1:c.1065C= (F12) XP_011532763.1:p.Gly355=
XM_011534462.1:c.729C= (F12) XP_011532764.1:p.Gly243=
XM_011534462.2:c.729C= (F12) XP_011532764.1:p.Gly243=
XM_017009773.2:c.1416+6970G= (SLC34A1) XP_016865262.1:n.1416+6970G=
NM_000505.4:c.1065C= (F12) MANE Select NP_000496.2:p.Gly355=