Canonical Allele Identifier: CA1603609114

Gene: F12 GRK6 SLC34A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404275G= , CM000667.2:g.177404275G=	GRCh38
NC_000005.9:g.176831276G= , CM000667.1:g.176831276G=	GRCh37
NC_000005.8:g.176763882G=	NCBI36
NG_007568.1:g.10302C= , LRG_145:g.10302C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*605C= (F12)	ENSP00000512476.1:n.*605C=
ENST00000696193.1:c.*1309C= (F12)	ENSP00000512477.1:n.*1309C=
ENST00000696194.1:c.*529C= (F12)	ENSP00000512478.1:n.*529C=
ENST00000696195.1:n.3742C= (F12)
ENST00000696200.1:n.1042C= (F12)
ENST00000696201.1:c.939C= (F12)	ENSP00000512482.1:p.Val313=
ENST00000253496.4:c.939C= (F12) MANE Select	ENSP00000253496.3:p.Val313=
ENST00000253496.3:c.939C= (F12)	ENSP00000253496.3:p.Val313=
ENST00000502598.5:c.-45+749G= (GRK6)	ENSP00000422873.1:n.-45+749G=
ENST00000502854.5:n.198C= (F12)
ENST00000503736.1:n.311C= (F12)
ENST00000510358.5:n.198C= (F12)
NM_000505.3:c.939C= , LRG_145t1:c.939C= (F12)	NP_000496.2:p.Val313=
XM_011534461.1:c.939C= (F12)	XP_011532763.1:p.Val313=
XM_011534462.1:c.603C= (F12)	XP_011532764.1:p.Val201=
XM_011534462.2:c.603C= (F12)	XP_011532764.1:p.Val201=
XM_017009773.2:c.1416+7201G= (SLC34A1)	XP_016865262.1:n.1416+7201G=
NM_000505.4:c.939C= (F12) MANE Select	NP_000496.2:p.Val313=