Canonical Allele Identifier: CA362326685

Gene: F12 GRK6 SLC34A1

Linked Data

• MyVariant Identifiers: chr5:g.176830884G>C (hg19) ; chr5:g.177403883G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177403883G>C , CM000667.2:g.177403883G>C	GRCh38
NC_000005.9:g.176830884G>C , CM000667.1:g.176830884G>C	GRCh37
NC_000005.8:g.176763490G>C	NCBI36
NG_007568.1:g.10694C>G , LRG_145:g.10694C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*892C>G (F12)	ENSP00000512476.1:n.*892C>G
ENST00000696193.1:c.*1613C>G (F12)	ENSP00000512477.1:n.*1613C>G
ENST00000696194.1:c.*816C>G (F12)	ENSP00000512478.1:n.*816C>G
ENST00000696195.1:n.4029C>G (F12)
ENST00000696200.1:n.1329C>G (F12)
ENST00000696201.1:c.1226C>G (F12)	ENSP00000512482.1:p.Thr409Arg
ENST00000253496.4:c.1226C>G (F12) MANE Select	ENSP00000253496.3:p.Thr409Arg
ENST00000253496.3:c.1226C>G (F12)	ENSP00000253496.3:p.Thr409Arg
ENST00000502598.5:c.-45+357G>C (GRK6)	ENSP00000422873.1:n.-45+357G>C
ENST00000502854.5:n.485C>G (F12)
ENST00000503736.1:n.598C>G (F12)
ENST00000510358.5:n.590C>G (F12)
NM_000505.3:c.1226C>G , LRG_145t1:c.1226C>G (F12)	NP_000496.2:p.Thr409Arg
XM_011534461.1:c.1226C>G (F12)	XP_011532763.1:p.Thr409Arg
XM_011534462.1:c.890C>G (F12)	XP_011532764.1:p.Thr297Arg
XM_011534462.2:c.890C>G (F12)	XP_011532764.1:p.Thr297Arg
XM_017009773.2:c.1416+6809G>C (SLC34A1)	XP_016865262.1:n.1416+6809G>C
NM_000505.4:c.1226C>G (F12) MANE Select	NP_000496.2:p.Thr409Arg