Canonical Allele Identifier: CA362327873

Gene: F12 GRK6 SLC34A1

Linked Data

• gnomAD v4: 5-177404046-C-A
• MyVariant Identifiers: chr5:g.176831047C>A (hg19) ; chr5:g.177404046C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404046C>A , CM000667.2:g.177404046C>A	GRCh38
NC_000005.9:g.176831047C>A , CM000667.1:g.176831047C>A	GRCh37
NC_000005.8:g.176763653C>A	NCBI36
NG_007568.1:g.10531G>T , LRG_145:g.10531G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696192.1:c.*729G>T (F12)	ENSP00000512476.1:n.*729G>T
ENST00000696193.1:c.*1450G>T (F12)	ENSP00000512477.1:n.*1450G>T
ENST00000696194.1:c.*653G>T (F12)	ENSP00000512478.1:n.*653G>T
ENST00000696195.1:n.3866G>T (F12)
ENST00000696200.1:n.1166G>T (F12)
ENST00000696201.1:c.1063G>T (F12)	ENSP00000512482.1:p.Gly355Cys
ENST00000253496.4:c.1063G>T (F12) MANE Select	ENSP00000253496.3:p.Gly355Cys
ENST00000253496.3:c.1063G>T (F12)	ENSP00000253496.3:p.Gly355Cys
ENST00000502598.5:c.-45+520C>A (GRK6)	ENSP00000422873.1:n.-45+520C>A
ENST00000502854.5:n.322G>T (F12)
ENST00000503736.1:n.435G>T (F12)
ENST00000510358.5:n.427G>T (F12)
NM_000505.3:c.1063G>T , LRG_145t1:c.1063G>T (F12)	NP_000496.2:p.Gly355Cys
XM_011534461.1:c.1063G>T (F12)	XP_011532763.1:p.Gly355Cys
XM_011534462.1:c.727G>T (F12)	XP_011532764.1:p.Gly243Cys
XM_011534462.2:c.727G>T (F12)	XP_011532764.1:p.Gly243Cys
XM_017009773.2:c.1416+6972C>A (SLC34A1)	XP_016865262.1:n.1416+6972C>A
NM_000505.4:c.1063G>T (F12) MANE Select	NP_000496.2:p.Gly355Cys