Canonical Allele Identifier: CA447964768

Gene: F12 GRK6 SLC34A1

Linked Data

• gnomAD v4: 5-177403942-C-A
• MyVariant Identifiers: chr5:g.176830943C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177403942C>A , CM000667.2:g.177403942C>A	GRCh38
NC_000005.9:g.176830943C>A , CM000667.1:g.176830943C>A	GRCh37
NC_000005.8:g.176763549C>A	NCBI36
NG_007568.1:g.10635G>T , LRG_145:g.10635G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*833G>T (F12)	ENSP00000512476.1:n.*833G>T
ENST00000696193.1:c.*1554G>T (F12)	ENSP00000512477.1:n.*1554G>T
ENST00000696194.1:c.*757G>T (F12)	ENSP00000512478.1:n.*757G>T
ENST00000696195.1:n.3970G>T (F12)
ENST00000696200.1:n.1270G>T (F12)
ENST00000696201.1:c.1167G>T (F12)	ENSP00000512482.1:p.Ala389=
ENST00000253496.4:c.1167G>T (F12) MANE Select	ENSP00000253496.3:p.Ala389=
ENST00000253496.3:c.1167G>T (F12)	ENSP00000253496.3:p.Ala389=
ENST00000502598.5:c.-45+416C>A (GRK6)	ENSP00000422873.1:n.-45+416C>A
ENST00000502854.5:n.426G>T (F12)
ENST00000503736.1:n.539G>T (F12)
ENST00000510358.5:n.531G>T (F12)
NM_000505.3:c.1167G>T , LRG_145t1:c.1167G>T (F12)	NP_000496.2:p.Ala389=
XM_011534461.1:c.1167G>T (F12)	XP_011532763.1:p.Ala389=
XM_011534462.1:c.831G>T (F12)	XP_011532764.1:p.Ala277=
XM_011534462.2:c.831G>T (F12)	XP_011532764.1:p.Ala277=
XM_017009773.2:c.1416+6868C>A (SLC34A1)	XP_016865262.1:n.1416+6868C>A
NM_000505.4:c.1167G>T (F12) MANE Select	NP_000496.2:p.Ala389=