Canonical Allele Identifier: CA1603609339

Gene: F12 GRK6 SLC34A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404393C= , CM000667.2:g.177404393C=	GRCh38
NC_000005.9:g.176831394C= , CM000667.1:g.176831394C=	GRCh37
NC_000005.8:g.176764000C=	NCBI36
NG_007568.1:g.10184G= , LRG_145:g.10184G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*487G= (F12)	ENSP00000512476.1:n.*487G=
ENST00000696193.1:c.*1191G= (F12)	ENSP00000512477.1:n.*1191G=
ENST00000696194.1:c.*411G= (F12)	ENSP00000512478.1:n.*411G=
ENST00000696195.1:n.3624G= (F12)
ENST00000696200.1:n.924G= (F12)
ENST00000696201.1:c.821G= (F12)	ENSP00000512482.1:p.Arg274=
ENST00000253496.4:c.821G= (F12) MANE Select	ENSP00000253496.3:p.Arg274=
ENST00000253496.3:c.821G= (F12)	ENSP00000253496.3:p.Arg274=
ENST00000502598.5:c.-45+867C= (GRK6)	ENSP00000422873.1:n.-45+867C=
ENST00000502854.5:n.80G= (F12)
ENST00000503736.1:n.193G= (F12)
ENST00000510358.5:n.80G= (F12)
NM_000505.3:c.821G= , LRG_145t1:c.821G= (F12)	NP_000496.2:p.Arg274=
XM_011534461.1:c.821G= (F12)	XP_011532763.1:p.Arg274=
XM_011534462.1:c.485G= (F12)	XP_011532764.1:p.Arg162=
XM_011534462.2:c.485G= (F12)	XP_011532764.1:p.Arg162=
XM_017009773.2:c.1416+7319C= (SLC34A1)	XP_016865262.1:n.1416+7319C=
NM_000505.4:c.821G= (F12) MANE Select	NP_000496.2:p.Arg274=