Canonical Allele Identifier: CA447728404

Gene: F12 GRK6 SLC34A1

Linked Data

• gnomAD v4: 5-177405981-G-T
• MyVariant Identifiers: chr5:g.176832982G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177405981G>T , CM000667.2:g.177405981G>T	GRCh38
NC_000005.9:g.176832982G>T , CM000667.1:g.176832982G>T	GRCh37
NC_000005.8:g.176765588G>T	NCBI36
NG_007568.1:g.8596C>A , LRG_145:g.8596C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.196C>A (F12)	ENSP00000512476.1:p.Arg66=
ENST00000696193.1:c.*120C>A (F12)	ENSP00000512477.1:n.*120C>A
ENST00000696194.1:c.196C>A (F12)	ENSP00000512478.1:p.Arg66=
ENST00000696195.1:n.2553C>A (F12)
ENST00000696200.1:n.299C>A (F12)
ENST00000696201.1:c.196C>A (F12)	ENSP00000512482.1:p.Arg66=
ENST00000253496.4:c.196C>A (F12) MANE Select	ENSP00000253496.3:p.Arg66=
ENST00000253496.3:c.196C>A (F12)	ENSP00000253496.3:p.Arg66=
ENST00000502598.5:c.-45+2455G>T (GRK6)	ENSP00000422873.1:n.-45+2455G>T
ENST00000506296.5:c.-45+1424G>T (GRK6)	ENSP00000421055.1:n.-45+1424G>T
NM_000505.3:c.196C>A , LRG_145t1:c.196C>A (F12)	NP_000496.2:p.Arg66=
XM_011534461.1:c.196C>A (F12)	XP_011532763.1:p.Arg66=
XM_017009773.2:c.1417-5783G>T (SLC34A1)	XP_016865262.1:n.1417-5783G>T
NM_000505.4:c.196C>A (F12) MANE Select	NP_000496.2:p.Arg66=