Canonical Allele Identifier: CA1603609678

Gene: F12 GRK6 SLC34A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404542C= , CM000667.2:g.177404542C=	GRCh38
NC_000005.9:g.176831543C= , CM000667.1:g.176831543C=	GRCh37
NC_000005.8:g.176764149C=	NCBI36
NG_007568.1:g.10035G= , LRG_145:g.10035G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*423G= (F12)	ENSP00000512476.1:n.*423G=
ENST00000696193.1:c.*1127G= (F12)	ENSP00000512477.1:n.*1127G=
ENST00000696194.1:c.*347G= (F12)	ENSP00000512478.1:n.*347G=
ENST00000696195.1:n.3560G= (F12)
ENST00000696200.1:n.860G= (F12)
ENST00000696201.1:c.757G= (F12)	ENSP00000512482.1:p.Glu253=
ENST00000253496.4:c.757G= (F12) MANE Select	ENSP00000253496.3:p.Glu253=
ENST00000253496.3:c.757G= (F12)	ENSP00000253496.3:p.Glu253=
ENST00000502598.5:c.-45+1016C= (GRK6)	ENSP00000422873.1:n.-45+1016C=
ENST00000503736.1:n.173-129G= (F12)
ENST00000506296.5:c.-60C= (GRK6)	ENSP00000421055.1:n.-60C=
NM_000505.3:c.757G= , LRG_145t1:c.757G= (F12)	NP_000496.2:p.Glu253=
XM_011534461.1:c.757G= (F12)	XP_011532763.1:p.Glu253=
XM_011534462.1:c.421G= (F12)	XP_011532764.1:p.Glu141=
XM_011534462.2:c.421G= (F12)	XP_011532764.1:p.Glu141=
XM_017009773.2:c.1417-7222C= (SLC34A1)	XP_016865262.1:n.1417-7222C=
NM_000505.4:c.757G= (F12) MANE Select	NP_000496.2:p.Glu253=