Canonical Allele Identifier: CA1603609801

Gene: F12 GRK6 SLC34A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404642A= , CM000667.2:g.177404642A=	GRCh38
NC_000005.9:g.176831643A= , CM000667.1:g.176831643A=	GRCh37
NC_000005.8:g.176764249A=	NCBI36
NG_007568.1:g.9935T= , LRG_145:g.9935T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*323T= (F12)	ENSP00000512476.1:n.*323T=
ENST00000696193.1:c.*1027T= (F12)	ENSP00000512477.1:n.*1027T=
ENST00000696194.1:c.*247T= (F12)	ENSP00000512478.1:n.*247T=
ENST00000696195.1:n.3460T= (F12)
ENST00000696200.1:n.760T= (F12)
ENST00000696201.1:c.657T= (F12)	ENSP00000512482.1:p.Asp219=
ENST00000253496.4:c.657T= (F12) MANE Select	ENSP00000253496.3:p.Asp219=
ENST00000253496.3:c.657T= (F12)	ENSP00000253496.3:p.Asp219=
ENST00000502598.5:c.-45+1116A= (GRK6)	ENSP00000422873.1:n.-45+1116A=
ENST00000503736.1:n.172+168T= (F12)
ENST00000506296.5:c.-45+85A= (GRK6)	ENSP00000421055.1:n.-45+85A=
NM_000505.3:c.657T= , LRG_145t1:c.657T= (F12)	NP_000496.2:p.Asp219=
XM_011534461.1:c.657T= (F12)	XP_011532763.1:p.Asp219=
XM_011534462.1:c.321T= (F12)	XP_011532764.1:p.Asp107=
XM_011534462.2:c.321T= (F12)	XP_011532764.1:p.Asp107=
XM_017009773.2:c.1417-7122A= (SLC34A1)	XP_016865262.1:n.1417-7122A=
NM_000505.4:c.657T= (F12) MANE Select	NP_000496.2:p.Asp219=