Canonical Allele Identifier: CA1603608449

Gene: F12 GRK6 SLC34A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177403645G= , CM000667.2:g.177403645G=	GRCh38
NC_000005.9:g.176830646G= , CM000667.1:g.176830646G=	GRCh37
NC_000005.8:g.176763252G=	NCBI36
NG_007568.1:g.10932C= , LRG_145:g.10932C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*917-28C= (F12)	ENSP00000512476.1:n.*917-28C=
ENST00000696193.1:c.*1638-28C= (F12)	ENSP00000512477.1:n.*1638-28C=
ENST00000696194.1:c.*841-28C= (F12)	ENSP00000512478.1:n.*841-28C=
ENST00000696195.1:n.4054-28C= (F12)
ENST00000696200.1:n.1567C= (F12)
ENST00000696201.1:c.1251-28C= (F12)	ENSP00000512482.1:n.1251-28C=
ENST00000253496.4:c.1251-28C= (F12) MANE Select	ENSP00000253496.3:n.1251-28C=
ENST00000253496.3:c.1251-28C= (F12)	ENSP00000253496.3:n.1251-28C=
ENST00000502598.5:c.-45+119G= (GRK6)	ENSP00000422873.1:n.-45+119G=
ENST00000502854.5:n.723C= (F12)
ENST00000503736.1:n.623-28C= (F12)
ENST00000504406.5:n.106C= (F12)
ENST00000510358.5:n.828C= (F12)
NM_000505.3:c.1251-28C= , LRG_145t1:c.1251-28C= (F12)	NP_000496.2:n.1251-28C=
XM_011534461.1:c.1251-28C= (F12)	XP_011532763.1:n.1251-28C=
XM_011534462.1:c.915-28C= (F12)	XP_011532764.1:n.915-28C=
XM_011534462.2:c.915-28C= (F12)	XP_011532764.1:n.915-28C=
XM_017009773.2:c.1416+6571G= (SLC34A1)	XP_016865262.1:n.1416+6571G=
NM_000505.4:c.1251-28C= (F12) MANE Select	NP_000496.2:n.1251-28C=