Canonical Allele Identifier: CA447964936

Gene: F12 GRK6 SLC34A1

Linked Data

• dbSNP Id: rs1763238535
• MyVariant Identifiers: chr5:g.176831607G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404606G>C , CM000667.2:g.177404606G>C	GRCh38
NC_000005.9:g.176831607G>C , CM000667.1:g.176831607G>C	GRCh37
NC_000005.8:g.176764213G>C	NCBI36
NG_007568.1:g.9971C>G , LRG_145:g.9971C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*359C>G (F12)	ENSP00000512476.1:n.*359C>G
ENST00000696193.1:c.*1063C>G (F12)	ENSP00000512477.1:n.*1063C>G
ENST00000696194.1:c.*283C>G (F12)	ENSP00000512478.1:n.*283C>G
ENST00000696195.1:n.3496C>G (F12)
ENST00000696200.1:n.796C>G (F12)
ENST00000696201.1:c.693C>G (F12)	ENSP00000512482.1:p.Thr231=
ENST00000253496.4:c.693C>G (F12) MANE Select	ENSP00000253496.3:p.Thr231=
ENST00000253496.3:c.693C>G (F12)	ENSP00000253496.3:p.Thr231=
ENST00000502598.5:c.-45+1080G>C (GRK6)	ENSP00000422873.1:n.-45+1080G>C
ENST00000503736.1:n.173-193C>G (F12)
ENST00000506296.5:c.-45+49G>C (GRK6)	ENSP00000421055.1:n.-45+49G>C
NM_000505.3:c.693C>G , LRG_145t1:c.693C>G (F12)	NP_000496.2:p.Thr231=
XM_011534461.1:c.693C>G (F12)	XP_011532763.1:p.Thr231=
XM_011534462.1:c.357C>G (F12)	XP_011532764.1:p.Thr119=
XM_011534462.2:c.357C>G (F12)	XP_011532764.1:p.Thr119=
XM_017009773.2:c.1417-7158G>C (SLC34A1)	XP_016865262.1:n.1417-7158G>C
NM_000505.4:c.693C>G (F12) MANE Select	NP_000496.2:p.Thr231=