Canonical Allele Identifier: CA2676711600

Gene: F12 GRK6 SLC34A1

Linked Data

• dbSNP Id: rs1763233246
• gnomAD v4: 5-177404483-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404483G>T , CM000667.2:g.177404483G>T	GRCh38
NC_000005.9:g.176831484G>T , CM000667.1:g.176831484G>T	GRCh37
NC_000005.8:g.176764090G>T	NCBI36
NG_007568.1:g.10094C>A , LRG_145:g.10094C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*466+16C>A (F12)	ENSP00000512476.1:n.*466+16C>A
ENST00000696193.1:c.*1170+16C>A (F12)	ENSP00000512477.1:n.*1170+16C>A
ENST00000696194.1:c.*390+16C>A (F12)	ENSP00000512478.1:n.*390+16C>A
ENST00000696195.1:n.3603+16C>A (F12)
ENST00000696200.1:n.903+16C>A (F12)
ENST00000696201.1:c.800+16C>A (F12)	ENSP00000512482.1:n.800+16C>A
ENST00000253496.4:c.800+16C>A (F12) MANE Select	ENSP00000253496.3:n.800+16C>A
ENST00000253496.3:c.800+16C>A (F12)	ENSP00000253496.3:n.800+16C>A
ENST00000502598.5:c.-45+957G>T (GRK6)	ENSP00000422873.1:n.-45+957G>T
ENST00000503736.1:n.173-70C>A (F12)
ENST00000506296.5:c.-119G>T (GRK6)	ENSP00000421055.1:n.-119G>T
NM_000505.3:c.800+16C>A , LRG_145t1:c.800+16C>A (F12)	NP_000496.2:n.800+16C>A
XM_011534461.1:c.800+16C>A (F12)	XP_011532763.1:n.800+16C>A
XM_011534462.1:c.464+16C>A (F12)	XP_011532764.1:n.464+16C>A
XM_011534462.2:c.464+16C>A (F12)	XP_011532764.1:n.464+16C>A
XM_017009773.2:c.1417-7281G>T (SLC34A1)	XP_016865262.1:n.1417-7281G>T
NM_000505.4:c.800+16C>A (F12) MANE Select	NP_000496.2:n.800+16C>A