Canonical Allele Identifier: CA1603609814

Gene: F12 GRK6 SLC34A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404646T= , CM000667.2:g.177404646T=	GRCh38
NC_000005.9:g.176831647T= , CM000667.1:g.176831647T=	GRCh37
NC_000005.8:g.176764253T=	NCBI36
NG_007568.1:g.9931A= , LRG_145:g.9931A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*319A= (F12)	ENSP00000512476.1:n.*319A=
ENST00000696193.1:c.*1023A= (F12)	ENSP00000512477.1:n.*1023A=
ENST00000696194.1:c.*243A= (F12)	ENSP00000512478.1:n.*243A=
ENST00000696195.1:n.3456A= (F12)
ENST00000696200.1:n.756A= (F12)
ENST00000696201.1:c.653A= (F12)	ENSP00000512482.1:p.Tyr218=
ENST00000253496.4:c.653A= (F12) MANE Select	ENSP00000253496.3:p.Tyr218=
ENST00000253496.3:c.653A= (F12)	ENSP00000253496.3:p.Tyr218=
ENST00000502598.5:c.-45+1120T= (GRK6)	ENSP00000422873.1:n.-45+1120T=
ENST00000503736.1:n.172+164A= (F12)
ENST00000506296.5:c.-45+89T= (GRK6)	ENSP00000421055.1:n.-45+89T=
NM_000505.3:c.653A= , LRG_145t1:c.653A= (F12)	NP_000496.2:p.Tyr218=
XM_011534461.1:c.653A= (F12)	XP_011532763.1:p.Tyr218=
XM_011534462.1:c.317A= (F12)	XP_011532764.1:p.Tyr106=
XM_011534462.2:c.317A= (F12)	XP_011532764.1:p.Tyr106=
XM_017009773.2:c.1417-7118T= (SLC34A1)	XP_016865262.1:n.1417-7118T=
NM_000505.4:c.653A= (F12) MANE Select	NP_000496.2:p.Tyr218=