Canonical Allele Identifier: CA1603608619

Gene: F12 GRK6 SLC34A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177403892C= , CM000667.2:g.177403892C=	GRCh38
NC_000005.9:g.176830893C= , CM000667.1:g.176830893C=	GRCh37
NC_000005.8:g.176763499C=	NCBI36
NG_007568.1:g.10685G= , LRG_145:g.10685G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*883G= (F12)	ENSP00000512476.1:n.*883G=
ENST00000696193.1:c.*1604G= (F12)	ENSP00000512477.1:n.*1604G=
ENST00000696194.1:c.*807G= (F12)	ENSP00000512478.1:n.*807G=
ENST00000696195.1:n.4020G= (F12)
ENST00000696200.1:n.1320G= (F12)
ENST00000696201.1:c.1217G= (F12)	ENSP00000512482.1:p.Trp406=
ENST00000253496.4:c.1217G= (F12) MANE Select	ENSP00000253496.3:p.Trp406=
ENST00000253496.3:c.1217G= (F12)	ENSP00000253496.3:p.Trp406=
ENST00000502598.5:c.-45+366C= (GRK6)	ENSP00000422873.1:n.-45+366C=
ENST00000502854.5:n.476G= (F12)
ENST00000503736.1:n.589G= (F12)
ENST00000510358.5:n.581G= (F12)
NM_000505.3:c.1217G= , LRG_145t1:c.1217G= (F12)	NP_000496.2:p.Trp406=
XM_011534461.1:c.1217G= (F12)	XP_011532763.1:p.Trp406=
XM_011534462.1:c.881G= (F12)	XP_011532764.1:p.Trp294=
XM_011534462.2:c.881G= (F12)	XP_011532764.1:p.Trp294=
XM_017009773.2:c.1416+6818C= (SLC34A1)	XP_016865262.1:n.1416+6818C=
NM_000505.4:c.1217G= (F12) MANE Select	NP_000496.2:p.Trp406=