Canonical Allele Identifier: CA362327978

Gene: F12 GRK6 SLC34A1

Linked Data

• gnomAD v4: 5-177404067-G-T
• MyVariant Identifiers: chr5:g.176831068G>T (hg19) ; chr5:g.177404067G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404067G>T , CM000667.2:g.177404067G>T	GRCh38
NC_000005.9:g.176831068G>T , CM000667.1:g.176831068G>T	GRCh37
NC_000005.8:g.176763674G>T	NCBI36
NG_007568.1:g.10510C>A , LRG_145:g.10510C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696192.1:c.*708C>A (F12)	ENSP00000512476.1:n.*708C>A
ENST00000696193.1:c.*1429C>A (F12)	ENSP00000512477.1:n.*1429C>A
ENST00000696194.1:c.*632C>A (F12)	ENSP00000512478.1:n.*632C>A
ENST00000696195.1:n.3845C>A (F12)
ENST00000696200.1:n.1145C>A (F12)
ENST00000696201.1:c.1042C>A (F12)	ENSP00000512482.1:p.Pro348Thr
ENST00000253496.4:c.1042C>A (F12) MANE Select	ENSP00000253496.3:p.Pro348Thr
ENST00000253496.3:c.1042C>A (F12)	ENSP00000253496.3:p.Pro348Thr
ENST00000502598.5:c.-45+541G>T (GRK6)	ENSP00000422873.1:n.-45+541G>T
ENST00000502854.5:n.301C>A (F12)
ENST00000503736.1:n.414C>A (F12)
ENST00000510358.5:n.406C>A (F12)
NM_000505.3:c.1042C>A , LRG_145t1:c.1042C>A (F12)	NP_000496.2:p.Pro348Thr
XM_011534461.1:c.1042C>A (F12)	XP_011532763.1:p.Pro348Thr
XM_011534462.1:c.706C>A (F12)	XP_011532764.1:p.Pro236Thr
XM_011534462.2:c.706C>A (F12)	XP_011532764.1:p.Pro236Thr
XM_017009773.2:c.1416+6993G>T (SLC34A1)	XP_016865262.1:n.1416+6993G>T
NM_000505.4:c.1042C>A (F12) MANE Select	NP_000496.2:p.Pro348Thr