Canonical Allele Identifier: CA362328596

Gene: F12 GRK6 SLC34A1

Linked Data

• MyVariant Identifiers: chr5:g.176831328T>C (hg19) ; chr5:g.177404327T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404327T>C , CM000667.2:g.177404327T>C	GRCh38
NC_000005.9:g.176831328T>C , CM000667.1:g.176831328T>C	GRCh37
NC_000005.8:g.176763934T>C	NCBI36
NG_007568.1:g.10250A>G , LRG_145:g.10250A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*553A>G (F12)	ENSP00000512476.1:n.*553A>G
ENST00000696193.1:c.*1257A>G (F12)	ENSP00000512477.1:n.*1257A>G
ENST00000696194.1:c.*477A>G (F12)	ENSP00000512478.1:n.*477A>G
ENST00000696195.1:n.3690A>G (F12)
ENST00000696200.1:n.990A>G (F12)
ENST00000696201.1:c.887A>G (F12)	ENSP00000512482.1:p.Gln296Arg
ENST00000253496.4:c.887A>G (F12) MANE Select	ENSP00000253496.3:p.Gln296Arg
ENST00000253496.3:c.887A>G (F12)	ENSP00000253496.3:p.Gln296Arg
ENST00000502598.5:c.-45+801T>C (GRK6)	ENSP00000422873.1:n.-45+801T>C
ENST00000502854.5:n.146A>G (F12)
ENST00000503736.1:n.259A>G (F12)
ENST00000510358.5:n.146A>G (F12)
NM_000505.3:c.887A>G , LRG_145t1:c.887A>G (F12)	NP_000496.2:p.Gln296Arg
XM_011534461.1:c.887A>G (F12)	XP_011532763.1:p.Gln296Arg
XM_011534462.1:c.551A>G (F12)	XP_011532764.1:p.Gln184Arg
XM_011534462.2:c.551A>G (F12)	XP_011532764.1:p.Gln184Arg
XM_017009773.2:c.1416+7253T>C (SLC34A1)	XP_016865262.1:n.1416+7253T>C
NM_000505.4:c.887A>G (F12) MANE Select	NP_000496.2:p.Gln296Arg