Canonical Allele Identifier: CA447964916

Gene: F12 GRK6 SLC34A1

Linked Data

• MyVariant Identifiers: chr5:g.176831026G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404025G>T , CM000667.2:g.177404025G>T	GRCh38
NC_000005.9:g.176831026G>T , CM000667.1:g.176831026G>T	GRCh37
NC_000005.8:g.176763632G>T	NCBI36
NG_007568.1:g.10552C>A , LRG_145:g.10552C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*750C>A (F12)	ENSP00000512476.1:n.*750C>A
ENST00000696193.1:c.*1471C>A (F12)	ENSP00000512477.1:n.*1471C>A
ENST00000696194.1:c.*674C>A (F12)	ENSP00000512478.1:n.*674C>A
ENST00000696195.1:n.3887C>A (F12)
ENST00000696200.1:n.1187C>A (F12)
ENST00000696201.1:c.1084C>A (F12)	ENSP00000512482.1:p.Arg362=
ENST00000253496.4:c.1084C>A (F12) MANE Select	ENSP00000253496.3:p.Arg362=
ENST00000253496.3:c.1084C>A (F12)	ENSP00000253496.3:p.Arg362=
ENST00000502598.5:c.-45+499G>T (GRK6)	ENSP00000422873.1:n.-45+499G>T
ENST00000502854.5:n.343C>A (F12)
ENST00000503736.1:n.456C>A (F12)
ENST00000510358.5:n.448C>A (F12)
NM_000505.3:c.1084C>A , LRG_145t1:c.1084C>A (F12)	NP_000496.2:p.Arg362=
XM_011534461.1:c.1084C>A (F12)	XP_011532763.1:p.Arg362=
XM_011534462.1:c.748C>A (F12)	XP_011532764.1:p.Arg250=
XM_011534462.2:c.748C>A (F12)	XP_011532764.1:p.Arg250=
XM_017009773.2:c.1416+6951G>T (SLC34A1)	XP_016865262.1:n.1416+6951G>T
NM_000505.4:c.1084C>A (F12) MANE Select	NP_000496.2:p.Arg362=