Canonical Allele Identifier: CA447965124

Gene: F12 GRK6 SLC34A1

Linked Data

• dbSNP Id: rs1488278711
• gnomAD v3: 5-177404074-C-T
• gnomAD v4: 5-177404074-C-T
• MyVariant Identifiers: chr5:g.176831075C>T (hg19) ; chr5:g.177404074C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404074C>T , CM000667.2:g.177404074C>T	GRCh38
NC_000005.9:g.176831075C>T , CM000667.1:g.176831075C>T	GRCh37
NC_000005.8:g.176763681C>T	NCBI36
NG_007568.1:g.10503G>A , LRG_145:g.10503G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696192.1:c.*701G>A (F12)	ENSP00000512476.1:n.*701G>A
ENST00000696193.1:c.*1422G>A (F12)	ENSP00000512477.1:n.*1422G>A
ENST00000696194.1:c.*625G>A (F12)	ENSP00000512478.1:n.*625G>A
ENST00000696195.1:n.3838G>A (F12)
ENST00000696200.1:n.1138G>A (F12)
ENST00000696201.1:c.1035G>A (F12)	ENSP00000512482.1:p.Arg345=
ENST00000253496.4:c.1035G>A (F12) MANE Select	ENSP00000253496.3:p.Arg345=
ENST00000253496.3:c.1035G>A (F12)	ENSP00000253496.3:p.Arg345=
ENST00000502598.5:c.-45+548C>T (GRK6)	ENSP00000422873.1:n.-45+548C>T
ENST00000502854.5:n.294G>A (F12)
ENST00000503736.1:n.407G>A (F12)
ENST00000510358.5:n.399G>A (F12)
NM_000505.3:c.1035G>A , LRG_145t1:c.1035G>A (F12)	NP_000496.2:p.Arg345=
XM_011534461.1:c.1035G>A (F12)	XP_011532763.1:p.Arg345=
XM_011534462.1:c.699G>A (F12)	XP_011532764.1:p.Arg233=
XM_011534462.2:c.699G>A (F12)	XP_011532764.1:p.Arg233=
XM_017009773.2:c.1416+7000C>T (SLC34A1)	XP_016865262.1:n.1416+7000C>T
NM_000505.4:c.1035G>A (F12) MANE Select	NP_000496.2:p.Arg345=