Canonical Allele Identifier: CA362329629

Gene: F12 GRK6 SLC34A1

Linked Data

• dbSNP Id: rs17876030
• gnomAD v4: 5-177404825-C-T
• MyVariant Identifiers: chr5:g.176831826C>T (hg19) ; chr5:g.177404825C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404825C>T , CM000667.2:g.177404825C>T	GRCh38
NC_000005.9:g.176831826C>T , CM000667.1:g.176831826C>T	GRCh37
NC_000005.8:g.176764432C>T	NCBI36
NG_007568.1:g.9752G>A , LRG_145:g.9752G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696192.1:c.*285G>A (F12)	ENSP00000512476.1:n.*285G>A
ENST00000696193.1:c.*844G>A (F12)	ENSP00000512477.1:n.*844G>A
ENST00000696194.1:c.*209G>A (F12)	ENSP00000512478.1:n.*209G>A
ENST00000696195.1:n.3277G>A (F12)
ENST00000696200.1:n.722G>A (F12)
ENST00000696201.1:c.619G>A (F12)	ENSP00000512482.1:p.Ala207Thr
ENST00000253496.4:c.619G>A (F12) MANE Select	ENSP00000253496.3:p.Ala207Thr
ENST00000253496.3:c.619G>A (F12)	ENSP00000253496.3:p.Ala207Thr
ENST00000502598.5:c.-45+1299C>T (GRK6)	ENSP00000422873.1:n.-45+1299C>T
ENST00000503736.1:n.157G>A (F12)
ENST00000506296.5:c.-45+268C>T (GRK6)	ENSP00000421055.1:n.-45+268C>T
NM_000505.3:c.619G>A , LRG_145t1:c.619G>A (F12)	NP_000496.2:p.Ala207Thr
XM_011534461.1:c.619G>A (F12)	XP_011532763.1:p.Ala207Thr
XM_011534462.1:c.283G>A (F12)	XP_011532764.1:p.Ala95Thr
XM_011534462.2:c.283G>A (F12)	XP_011532764.1:p.Ala95Thr
XM_017009773.2:c.1417-6939C>T (SLC34A1)	XP_016865262.1:n.1417-6939C>T
NM_000505.4:c.619G>A (F12) MANE Select	NP_000496.2:p.Ala207Thr