Canonical Allele Identifier: CA447965090

Gene: F12 GRK6 SLC34A1

Linked Data

• gnomAD v4: 5-177404557-G-T
• MyVariant Identifiers: chr5:g.176831558G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404557G>T , CM000667.2:g.177404557G>T	GRCh38
NC_000005.9:g.176831558G>T , CM000667.1:g.176831558G>T	GRCh37
NC_000005.8:g.176764164G>T	NCBI36
NG_007568.1:g.10020C>A , LRG_145:g.10020C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*408C>A (F12)	ENSP00000512476.1:n.*408C>A
ENST00000696193.1:c.*1112C>A (F12)	ENSP00000512477.1:n.*1112C>A
ENST00000696194.1:c.*332C>A (F12)	ENSP00000512478.1:n.*332C>A
ENST00000696195.1:n.3545C>A (F12)
ENST00000696200.1:n.845C>A (F12)
ENST00000696201.1:c.742C>A (F12)	ENSP00000512482.1:p.Arg248=
ENST00000253496.4:c.742C>A (F12) MANE Select	ENSP00000253496.3:p.Arg248=
ENST00000253496.3:c.742C>A (F12)	ENSP00000253496.3:p.Arg248=
ENST00000502598.5:c.-45+1031G>T (GRK6)	ENSP00000422873.1:n.-45+1031G>T
ENST00000503736.1:n.173-144C>A (F12)
ENST00000506296.5:c.-45G>T (GRK6)	ENSP00000421055.1:n.-45G>T
NM_000505.3:c.742C>A , LRG_145t1:c.742C>A (F12)	NP_000496.2:p.Arg248=
XM_011534461.1:c.742C>A (F12)	XP_011532763.1:p.Arg248=
XM_011534462.1:c.406C>A (F12)	XP_011532764.1:p.Arg136=
XM_011534462.2:c.406C>A (F12)	XP_011532764.1:p.Arg136=
XM_017009773.2:c.1417-7207G>T (SLC34A1)	XP_016865262.1:n.1417-7207G>T
NM_000505.4:c.742C>A (F12) MANE Select	NP_000496.2:p.Arg248=