Canonical Allele Identifier: CA1603620014

Gene: F12 GRK6 SLC34A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177409531A= , CM000667.2:g.177409531A=	GRCh38
NC_000005.9:g.176836532A= , CM000667.1:g.176836532A=	GRCh37
NC_000005.8:g.176769138A=	NCBI36
NG_007568.1:g.5046T= , LRG_145:g.5046T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000505.4:c.-4T= (F12) MANE Select	NP_000496.2:n.-4T=
ENST00000253496.4:c.-4T= (F12) MANE Select	ENSP00000253496.3:n.-4T=
NM_000505.3:c.-4T= , LRG_145t1:c.-4T= (F12)	NP_000496.2:n.-4T=
ENST00000253496.3:c.-4T= (F12)	ENSP00000253496.3:n.-4T=
ENST00000502598.5:c.-45+6005A= (GRK6)	ENSP00000422873.1:n.-45+6005A=
ENST00000506296.5:c.-45+4974A= (GRK6)	ENSP00000421055.1:n.-45+4974A=
ENST00000696192.1:c.-4T= (F12)	ENSP00000512476.1:n.-4T=
ENST00000696193.1:c.-4T= (F12)	ENSP00000512477.1:n.-4T=
ENST00000696194.1:c.-4T= (F12)	ENSP00000512478.1:n.-4T=
ENST00000696195.1:n.45T= (F12)
ENST00000696200.1:n.100T= (F12)
ENST00000696201.1:c.-4T= (F12)	ENSP00000512482.1:n.-4T=
XM_011534461.1:c.-4T= (F12)	XP_011532763.1:n.-4T=
XM_017009773.2:c.1417-2233A= (SLC34A1)	XP_016865262.1:n.1417-2233A=