Canonical Allele Identifier: CA447964795

Gene: F12 GRK6 SLC34A1

Linked Data

• gnomAD v4: 5-177403963-C-T
• MyVariant Identifiers: chr5:g.176830964C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177403963C>T , CM000667.2:g.177403963C>T	GRCh38
NC_000005.9:g.176830964C>T , CM000667.1:g.176830964C>T	GRCh37
NC_000005.8:g.176763570C>T	NCBI36
NG_007568.1:g.10614G>A , LRG_145:g.10614G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*812G>A (F12)	ENSP00000512476.1:n.*812G>A
ENST00000696193.1:c.*1533G>A (F12)	ENSP00000512477.1:n.*1533G>A
ENST00000696194.1:c.*736G>A (F12)	ENSP00000512478.1:n.*736G>A
ENST00000696195.1:n.3949G>A (F12)
ENST00000696200.1:n.1249G>A (F12)
ENST00000696201.1:c.1146G>A (F12)	ENSP00000512482.1:p.Gly382=
ENST00000253496.4:c.1146G>A (F12) MANE Select	ENSP00000253496.3:p.Gly382=
ENST00000253496.3:c.1146G>A (F12)	ENSP00000253496.3:p.Gly382=
ENST00000502598.5:c.-45+437C>T (GRK6)	ENSP00000422873.1:n.-45+437C>T
ENST00000502854.5:n.405G>A (F12)
ENST00000503736.1:n.518G>A (F12)
ENST00000510358.5:n.510G>A (F12)
NM_000505.3:c.1146G>A , LRG_145t1:c.1146G>A (F12)	NP_000496.2:p.Gly382=
XM_011534461.1:c.1146G>A (F12)	XP_011532763.1:p.Gly382=
XM_011534462.1:c.810G>A (F12)	XP_011532764.1:p.Gly270=
XM_011534462.2:c.810G>A (F12)	XP_011532764.1:p.Gly270=
XM_017009773.2:c.1416+6889C>T (SLC34A1)	XP_016865262.1:n.1416+6889C>T
NM_000505.4:c.1146G>A (F12) MANE Select	NP_000496.2:p.Gly382=