Canonical Allele Identifier: CA1603609098

Gene: F12 GRK6 SLC34A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404264G= , CM000667.2:g.177404264G=	GRCh38
NC_000005.9:g.176831265G= , CM000667.1:g.176831265G=	GRCh37
NC_000005.8:g.176763871G=	NCBI36
NG_007568.1:g.10313C= , LRG_145:g.10313C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*616C= (F12)	ENSP00000512476.1:n.*616C=
ENST00000696193.1:c.*1320C= (F12)	ENSP00000512477.1:n.*1320C=
ENST00000696194.1:c.*540C= (F12)	ENSP00000512478.1:n.*540C=
ENST00000696195.1:n.3753C= (F12)
ENST00000696200.1:n.1053C= (F12)
ENST00000696201.1:c.950C= (F12)	ENSP00000512482.1:p.Pro317=
ENST00000253496.4:c.950C= (F12) MANE Select	ENSP00000253496.3:p.Pro317=
ENST00000253496.3:c.950C= (F12)	ENSP00000253496.3:p.Pro317=
ENST00000502598.5:c.-45+738G= (GRK6)	ENSP00000422873.1:n.-45+738G=
ENST00000502854.5:n.209C= (F12)
ENST00000503736.1:n.322C= (F12)
ENST00000510358.5:n.209C= (F12)
NM_000505.3:c.950C= , LRG_145t1:c.950C= (F12)	NP_000496.2:p.Pro317=
XM_011534461.1:c.950C= (F12)	XP_011532763.1:p.Pro317=
XM_011534462.1:c.614C= (F12)	XP_011532764.1:p.Pro205=
XM_011534462.2:c.614C= (F12)	XP_011532764.1:p.Pro205=
XM_017009773.2:c.1416+7190G= (SLC34A1)	XP_016865262.1:n.1416+7190G=
NM_000505.4:c.950C= (F12) MANE Select	NP_000496.2:p.Pro317=