Canonical Allele Identifier: CA1603608803

Gene: F12 GRK6 SLC34A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404085G= , CM000667.2:g.177404085G=	GRCh38
NC_000005.9:g.176831086G= , CM000667.1:g.176831086G=	GRCh37
NC_000005.8:g.176763692G=	NCBI36
NG_007568.1:g.10492C= , LRG_145:g.10492C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696192.1:c.*690C= (F12)	ENSP00000512476.1:n.*690C=
ENST00000696193.1:c.*1411C= (F12)	ENSP00000512477.1:n.*1411C=
ENST00000696194.1:c.*614C= (F12)	ENSP00000512478.1:n.*614C=
ENST00000696195.1:n.3827C= (F12)
ENST00000696200.1:n.1127C= (F12)
ENST00000696201.1:c.1024C= (F12)	ENSP00000512482.1:p.Pro342=
ENST00000253496.4:c.1024C= (F12) MANE Select	ENSP00000253496.3:p.Pro342=
ENST00000253496.3:c.1024C= (F12)	ENSP00000253496.3:p.Pro342=
ENST00000502598.5:c.-45+559G= (GRK6)	ENSP00000422873.1:n.-45+559G=
ENST00000502854.5:n.283C= (F12)
ENST00000503736.1:n.396C= (F12)
ENST00000510358.5:n.388C= (F12)
NM_000505.3:c.1024C= , LRG_145t1:c.1024C= (F12)	NP_000496.2:p.Pro342=
XM_011534461.1:c.1024C= (F12)	XP_011532763.1:p.Pro342=
XM_011534462.1:c.688C= (F12)	XP_011532764.1:p.Pro230=
XM_011534462.2:c.688C= (F12)	XP_011532764.1:p.Pro230=
XM_017009773.2:c.1416+7011G= (SLC34A1)	XP_016865262.1:n.1416+7011G=
NM_000505.4:c.1024C= (F12) MANE Select	NP_000496.2:p.Pro342=