Canonical Allele Identifier: CA447965152

Gene: F12 GRK6 SLC34A1

Linked Data

• gnomAD v4: 5-177404591-C-T
• MyVariant Identifiers: chr5:g.176831592C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404591C>T , CM000667.2:g.177404591C>T	GRCh38
NC_000005.9:g.176831592C>T , CM000667.1:g.176831592C>T	GRCh37
NC_000005.8:g.176764198C>T	NCBI36
NG_007568.1:g.9986G>A , LRG_145:g.9986G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*374G>A (F12)	ENSP00000512476.1:n.*374G>A
ENST00000696193.1:c.*1078G>A (F12)	ENSP00000512477.1:n.*1078G>A
ENST00000696194.1:c.*298G>A (F12)	ENSP00000512478.1:n.*298G>A
ENST00000696195.1:n.3511G>A (F12)
ENST00000696200.1:n.811G>A (F12)
ENST00000696201.1:c.708G>A (F12)	ENSP00000512482.1:p.Ala236=
ENST00000253496.4:c.708G>A (F12) MANE Select	ENSP00000253496.3:p.Ala236=
ENST00000253496.3:c.708G>A (F12)	ENSP00000253496.3:p.Ala236=
ENST00000502598.5:c.-45+1065C>T (GRK6)	ENSP00000422873.1:n.-45+1065C>T
ENST00000503736.1:n.173-178G>A (F12)
ENST00000506296.5:c.-45+34C>T (GRK6)	ENSP00000421055.1:n.-45+34C>T
NM_000505.3:c.708G>A , LRG_145t1:c.708G>A (F12)	NP_000496.2:p.Ala236=
XM_011534461.1:c.708G>A (F12)	XP_011532763.1:p.Ala236=
XM_011534462.1:c.372G>A (F12)	XP_011532764.1:p.Ala124=
XM_011534462.2:c.372G>A (F12)	XP_011532764.1:p.Ala124=
XM_017009773.2:c.1417-7173C>T (SLC34A1)	XP_016865262.1:n.1417-7173C>T
NM_000505.4:c.708G>A (F12) MANE Select	NP_000496.2:p.Ala236=