Canonical Allele Identifier: CA362328286

Gene: F12 GRK6 SLC34A1

Linked Data

• gnomAD v4: 5-177404235-G-T
• MyVariant Identifiers: chr5:g.176831236G>T (hg19) ; chr5:g.177404235G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404235G>T , CM000667.2:g.177404235G>T	GRCh38
NC_000005.9:g.176831236G>T , CM000667.1:g.176831236G>T	GRCh37
NC_000005.8:g.176763842G>T	NCBI36
NG_007568.1:g.10342C>A , LRG_145:g.10342C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696192.1:c.*645C>A (F12)	ENSP00000512476.1:n.*645C>A
ENST00000696193.1:c.*1349C>A (F12)	ENSP00000512477.1:n.*1349C>A
ENST00000696194.1:c.*569C>A (F12)	ENSP00000512478.1:n.*569C>A
ENST00000696195.1:n.3782C>A (F12)
ENST00000696200.1:n.1082C>A (F12)
ENST00000696201.1:c.979C>A (F12)	ENSP00000512482.1:p.Pro327Thr
ENST00000253496.4:c.979C>A (F12) MANE Select	ENSP00000253496.3:p.Pro327Thr
ENST00000253496.3:c.979C>A (F12)	ENSP00000253496.3:p.Pro327Thr
ENST00000502598.5:c.-45+709G>T (GRK6)	ENSP00000422873.1:n.-45+709G>T
ENST00000502854.5:n.238C>A (F12)
ENST00000503736.1:n.351C>A (F12)
ENST00000510358.5:n.238C>A (F12)
NM_000505.3:c.979C>A , LRG_145t1:c.979C>A (F12)	NP_000496.2:p.Pro327Thr
XM_011534461.1:c.979C>A (F12)	XP_011532763.1:p.Pro327Thr
XM_011534462.1:c.643C>A (F12)	XP_011532764.1:p.Pro215Thr
XM_011534462.2:c.643C>A (F12)	XP_011532764.1:p.Pro215Thr
XM_017009773.2:c.1416+7161G>T (SLC34A1)	XP_016865262.1:n.1416+7161G>T
NM_000505.4:c.979C>A (F12) MANE Select	NP_000496.2:p.Pro327Thr