Canonical Allele Identifier: CA1603608836

Gene: F12 GRK6 SLC34A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404131G= , CM000667.2:g.177404131G=	GRCh38
NC_000005.9:g.176831132G= , CM000667.1:g.176831132G=	GRCh37
NC_000005.8:g.176763738G=	NCBI36
NG_007568.1:g.10446C= , LRG_145:g.10446C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696192.1:c.*685-41C= (F12)	ENSP00000512476.1:n.*685-41C=
ENST00000696193.1:c.*1389-24C= (F12)	ENSP00000512477.1:n.*1389-24C=
ENST00000696194.1:c.*609-41C= (F12)	ENSP00000512478.1:n.*609-41C=
ENST00000696195.1:n.3822-41C= (F12)
ENST00000696200.1:n.1122-41C= (F12)
ENST00000696201.1:c.1019-41C= (F12)	ENSP00000512482.1:n.1019-41C=
ENST00000253496.4:c.1019-41C= (F12) MANE Select	ENSP00000253496.3:n.1019-41C=
ENST00000253496.3:c.1019-41C= (F12)	ENSP00000253496.3:n.1019-41C=
ENST00000502598.5:c.-45+605G= (GRK6)	ENSP00000422873.1:n.-45+605G=
ENST00000502854.5:n.278-41C= (F12)
ENST00000503736.1:n.391-41C= (F12)
ENST00000510358.5:n.342C= (F12)
NM_000505.3:c.1019-41C= , LRG_145t1:c.1019-41C= (F12)	NP_000496.2:n.1019-41C=
XM_011534461.1:c.1019-41C= (F12)	XP_011532763.1:n.1019-41C=
XM_011534462.1:c.683-41C= (F12)	XP_011532764.1:n.683-41C=
XM_011534462.2:c.683-41C= (F12)	XP_011532764.1:n.683-41C=
XM_017009773.2:c.1416+7057G= (SLC34A1)	XP_016865262.1:n.1416+7057G=
NM_000505.4:c.1019-41C= (F12) MANE Select	NP_000496.2:n.1019-41C=