Canonical Allele Identifier: CA1603609565

Gene: F12 GRK6 SLC34A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404500G= , CM000667.2:g.177404500G=	GRCh38
NC_000005.9:g.176831501G= , CM000667.1:g.176831501G=	GRCh37
NC_000005.8:g.176764107G=	NCBI36
NG_007568.1:g.10077C= , LRG_145:g.10077C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*465C= (F12)	ENSP00000512476.1:n.*465C=
ENST00000696193.1:c.*1169C= (F12)	ENSP00000512477.1:n.*1169C=
ENST00000696194.1:c.*389C= (F12)	ENSP00000512478.1:n.*389C=
ENST00000696195.1:n.3602C= (F12)
ENST00000696200.1:n.902C= (F12)
ENST00000696201.1:c.799C= (F12)	ENSP00000512482.1:p.Arg267=
ENST00000253496.4:c.799C= (F12) MANE Select	ENSP00000253496.3:p.Arg267=
ENST00000253496.3:c.799C= (F12)	ENSP00000253496.3:p.Arg267=
ENST00000502598.5:c.-45+974G= (GRK6)	ENSP00000422873.1:n.-45+974G=
ENST00000503736.1:n.173-87C= (F12)
ENST00000506296.5:c.-102G= (GRK6)	ENSP00000421055.1:n.-102G=
NM_000505.3:c.799C= , LRG_145t1:c.799C= (F12)	NP_000496.2:p.Arg267=
XM_011534461.1:c.799C= (F12)	XP_011532763.1:p.Arg267=
XM_011534462.1:c.463C= (F12)	XP_011532764.1:p.Arg155=
XM_011534462.2:c.463C= (F12)	XP_011532764.1:p.Arg155=
XM_017009773.2:c.1417-7264G= (SLC34A1)	XP_016865262.1:n.1417-7264G=
NM_000505.4:c.799C= (F12) MANE Select	NP_000496.2:p.Arg267=