Canonical Allele Identifier: CA447964840

Gene: F12 GRK6 SLC34A1

Linked Data

• gnomAD v4: 5-177403987-A-G
• MyVariant Identifiers: chr5:g.176830988A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177403987A>G , CM000667.2:g.177403987A>G	GRCh38
NC_000005.9:g.176830988A>G , CM000667.1:g.176830988A>G	GRCh37
NC_000005.8:g.176763594A>G	NCBI36
NG_007568.1:g.10590T>C , LRG_145:g.10590T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*788T>C (F12)	ENSP00000512476.1:n.*788T>C
ENST00000696193.1:c.*1509T>C (F12)	ENSP00000512477.1:n.*1509T>C
ENST00000696194.1:c.*712T>C (F12)	ENSP00000512478.1:n.*712T>C
ENST00000696195.1:n.3925T>C (F12)
ENST00000696200.1:n.1225T>C (F12)
ENST00000696201.1:c.1122T>C (F12)	ENSP00000512482.1:p.Val374=
ENST00000253496.4:c.1122T>C (F12) MANE Select	ENSP00000253496.3:p.Val374=
ENST00000253496.3:c.1122T>C (F12)	ENSP00000253496.3:p.Val374=
ENST00000502598.5:c.-45+461A>G (GRK6)	ENSP00000422873.1:n.-45+461A>G
ENST00000502854.5:n.381T>C (F12)
ENST00000503736.1:n.494T>C (F12)
ENST00000510358.5:n.486T>C (F12)
NM_000505.3:c.1122T>C , LRG_145t1:c.1122T>C (F12)	NP_000496.2:p.Val374=
XM_011534461.1:c.1122T>C (F12)	XP_011532763.1:p.Val374=
XM_011534462.1:c.786T>C (F12)	XP_011532764.1:p.Val262=
XM_011534462.2:c.786T>C (F12)	XP_011532764.1:p.Val262=
XM_017009773.2:c.1416+6913A>G (SLC34A1)	XP_016865262.1:n.1416+6913A>G
NM_000505.4:c.1122T>C (F12) MANE Select	NP_000496.2:p.Val374=