Canonical Allele Identifier: CA1603609795

Gene: F12 GRK6 SLC34A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404636G= , CM000667.2:g.177404636G=	GRCh38
NC_000005.9:g.176831637G= , CM000667.1:g.176831637G=	GRCh37
NC_000005.8:g.176764243G=	NCBI36
NG_007568.1:g.9941C= , LRG_145:g.9941C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*329C= (F12)	ENSP00000512476.1:n.*329C=
ENST00000696193.1:c.*1033C= (F12)	ENSP00000512477.1:n.*1033C=
ENST00000696194.1:c.*253C= (F12)	ENSP00000512478.1:n.*253C=
ENST00000696195.1:n.3466C= (F12)
ENST00000696200.1:n.766C= (F12)
ENST00000696201.1:c.663C= (F12)	ENSP00000512482.1:p.Arg221=
ENST00000253496.4:c.663C= (F12) MANE Select	ENSP00000253496.3:p.Arg221=
ENST00000253496.3:c.663C= (F12)	ENSP00000253496.3:p.Arg221=
ENST00000502598.5:c.-45+1110G= (GRK6)	ENSP00000422873.1:n.-45+1110G=
ENST00000503736.1:n.172+174C= (F12)
ENST00000506296.5:c.-45+79G= (GRK6)	ENSP00000421055.1:n.-45+79G=
NM_000505.3:c.663C= , LRG_145t1:c.663C= (F12)	NP_000496.2:p.Arg221=
XM_011534461.1:c.663C= (F12)	XP_011532763.1:p.Arg221=
XM_011534462.1:c.327C= (F12)	XP_011532764.1:p.Arg109=
XM_011534462.2:c.327C= (F12)	XP_011532764.1:p.Arg109=
XM_017009773.2:c.1417-7128G= (SLC34A1)	XP_016865262.1:n.1417-7128G=
NM_000505.4:c.663C= (F12) MANE Select	NP_000496.2:p.Arg221=