Canonical Allele Identifier: CA447964703

Gene: F12 GRK6 SLC34A1

Linked Data

• gnomAD v4: 5-177403885-C-A
• MyVariant Identifiers: chr5:g.176830886C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177403885C>A , CM000667.2:g.177403885C>A	GRCh38
NC_000005.9:g.176830886C>A , CM000667.1:g.176830886C>A	GRCh37
NC_000005.8:g.176763492C>A	NCBI36
NG_007568.1:g.10692G>T , LRG_145:g.10692G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*890G>T (F12)	ENSP00000512476.1:n.*890G>T
ENST00000696193.1:c.*1611G>T (F12)	ENSP00000512477.1:n.*1611G>T
ENST00000696194.1:c.*814G>T (F12)	ENSP00000512478.1:n.*814G>T
ENST00000696195.1:n.4027G>T (F12)
ENST00000696200.1:n.1327G>T (F12)
ENST00000696201.1:c.1224G>T (F12)	ENSP00000512482.1:p.Leu408=
ENST00000253496.4:c.1224G>T (F12) MANE Select	ENSP00000253496.3:p.Leu408=
ENST00000253496.3:c.1224G>T (F12)	ENSP00000253496.3:p.Leu408=
ENST00000502598.5:c.-45+359C>A (GRK6)	ENSP00000422873.1:n.-45+359C>A
ENST00000502854.5:n.483G>T (F12)
ENST00000503736.1:n.596G>T (F12)
ENST00000510358.5:n.588G>T (F12)
NM_000505.3:c.1224G>T , LRG_145t1:c.1224G>T (F12)	NP_000496.2:p.Leu408=
XM_011534461.1:c.1224G>T (F12)	XP_011532763.1:p.Leu408=
XM_011534462.1:c.888G>T (F12)	XP_011532764.1:p.Leu296=
XM_011534462.2:c.888G>T (F12)	XP_011532764.1:p.Leu296=
XM_017009773.2:c.1416+6811C>A (SLC34A1)	XP_016865262.1:n.1416+6811C>A
NM_000505.4:c.1224G>T (F12) MANE Select	NP_000496.2:p.Leu408=