Canonical Allele Identifier: CA1603608957

Gene: F12 GRK6 SLC34A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404192T= , CM000667.2:g.177404192T=	GRCh38
NC_000005.9:g.176831193T= , CM000667.1:g.176831193T=	GRCh37
NC_000005.8:g.176763799T=	NCBI36
NG_007568.1:g.10385A= , LRG_145:g.10385A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*684+4A= (F12)	ENSP00000512476.1:n.*684+4A=
ENST00000696193.1:c.*1388+4A= (F12)	ENSP00000512477.1:n.*1388+4A=
ENST00000696194.1:c.*608+4A= (F12)	ENSP00000512478.1:n.*608+4A=
ENST00000696195.1:n.3821+4A= (F12)
ENST00000696200.1:n.1121+4A= (F12)
ENST00000696201.1:c.1018+4A= (F12)	ENSP00000512482.1:n.1018+4A=
ENST00000253496.4:c.1018+4A= (F12) MANE Select	ENSP00000253496.3:n.1018+4A=
ENST00000253496.3:c.1018+4A= (F12)	ENSP00000253496.3:n.1018+4A=
ENST00000502598.5:c.-45+666T= (GRK6)	ENSP00000422873.1:n.-45+666T=
ENST00000502854.5:n.277+4A= (F12)
ENST00000503736.1:n.390+4A= (F12)
ENST00000510358.5:n.281A= (F12)
NM_000505.3:c.1018+4A= , LRG_145t1:c.1018+4A= (F12)	NP_000496.2:n.1018+4A=
XM_011534461.1:c.1018+4A= (F12)	XP_011532763.1:n.1018+4A=
XM_011534462.1:c.682+4A= (F12)	XP_011532764.1:n.682+4A=
XM_011534462.2:c.682+4A= (F12)	XP_011532764.1:n.682+4A=
XM_017009773.2:c.1416+7118T= (SLC34A1)	XP_016865262.1:n.1416+7118T=
NM_000505.4:c.1018+4A= (F12) MANE Select	NP_000496.2:n.1018+4A=