Canonical Allele Identifier: CA1603609783

Gene: F12 GRK6 SLC34A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404623G= , CM000667.2:g.177404623G=	GRCh38
NC_000005.9:g.176831624G= , CM000667.1:g.176831624G=	GRCh37
NC_000005.8:g.176764230G=	NCBI36
NG_007568.1:g.9954C= , LRG_145:g.9954C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*342C= (F12)	ENSP00000512476.1:n.*342C=
ENST00000696193.1:c.*1046C= (F12)	ENSP00000512477.1:n.*1046C=
ENST00000696194.1:c.*266C= (F12)	ENSP00000512478.1:n.*266C=
ENST00000696195.1:n.3479C= (F12)
ENST00000696200.1:n.779C= (F12)
ENST00000696201.1:c.676C= (F12)	ENSP00000512482.1:p.Arg226=
ENST00000253496.4:c.676C= (F12) MANE Select	ENSP00000253496.3:p.Arg226=
ENST00000253496.3:c.676C= (F12)	ENSP00000253496.3:p.Arg226=
ENST00000502598.5:c.-45+1097G= (GRK6)	ENSP00000422873.1:n.-45+1097G=
ENST00000503736.1:n.172+187C= (F12)
ENST00000506296.5:c.-45+66G= (GRK6)	ENSP00000421055.1:n.-45+66G=
NM_000505.3:c.676C= , LRG_145t1:c.676C= (F12)	NP_000496.2:p.Arg226=
XM_011534461.1:c.676C= (F12)	XP_011532763.1:p.Arg226=
XM_011534462.1:c.340C= (F12)	XP_011532764.1:p.Arg114=
XM_011534462.2:c.340C= (F12)	XP_011532764.1:p.Arg114=
XM_017009773.2:c.1417-7141G= (SLC34A1)	XP_016865262.1:n.1417-7141G=
NM_000505.4:c.676C= (F12) MANE Select	NP_000496.2:p.Arg226=