Canonical Allele Identifier: CA362328257

Gene: F12 GRK6 SLC34A1

Linked Data

• MyVariant Identifiers: chr5:g.176831226C>G (hg19) ; chr5:g.177404225C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404225C>G , CM000667.2:g.177404225C>G	GRCh38
NC_000005.9:g.176831226C>G , CM000667.1:g.176831226C>G	GRCh37
NC_000005.8:g.176763832C>G	NCBI36
NG_007568.1:g.10352G>C , LRG_145:g.10352G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*655G>C (F12)	ENSP00000512476.1:n.*655G>C
ENST00000696193.1:c.*1359G>C (F12)	ENSP00000512477.1:n.*1359G>C
ENST00000696194.1:c.*579G>C (F12)	ENSP00000512478.1:n.*579G>C
ENST00000696195.1:n.3792G>C (F12)
ENST00000696200.1:n.1092G>C (F12)
ENST00000696201.1:c.989G>C (F12)	ENSP00000512482.1:p.Arg330Pro
ENST00000253496.4:c.989G>C (F12) MANE Select	ENSP00000253496.3:p.Arg330Pro
ENST00000253496.3:c.989G>C (F12)	ENSP00000253496.3:p.Arg330Pro
ENST00000502598.5:c.-45+699C>G (GRK6)	ENSP00000422873.1:n.-45+699C>G
ENST00000502854.5:n.248G>C (F12)
ENST00000503736.1:n.361G>C (F12)
ENST00000510358.5:n.248G>C (F12)
NM_000505.3:c.989G>C , LRG_145t1:c.989G>C (F12)	NP_000496.2:p.Arg330Pro
XM_011534461.1:c.989G>C (F12)	XP_011532763.1:p.Arg330Pro
XM_011534462.1:c.653G>C (F12)	XP_011532764.1:p.Arg218Pro
XM_011534462.2:c.653G>C (F12)	XP_011532764.1:p.Arg218Pro
XM_017009773.2:c.1416+7151C>G (SLC34A1)	XP_016865262.1:n.1416+7151C>G
NM_000505.4:c.989G>C (F12) MANE Select	NP_000496.2:p.Arg330Pro