Canonical Allele Identifier: CA3038604600

Gene: F12 GRK6 SLC34A1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404133_177404134insAC , CM000667.2:g.177404133_177404134insAC	GRCh38
NC_000005.9:g.176831134_176831135insAC , CM000667.1:g.176831134_176831135insAC	GRCh37
NC_000005.8:g.176763740_176763741insAC	NCBI36
NG_007568.1:g.10444_10445insTG , LRG_145:g.10444_10445insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*685-43_*685-42insTG (F12)	ENSP00000512476.1:n.*685-43_*685-42insTG
ENST00000696193.1:c.*1389-26_*1389-25insTG (F12)	ENSP00000512477.1:n.*1389-26_*1389-25insTG
ENST00000696194.1:c.*609-43_*609-42insTG (F12)	ENSP00000512478.1:n.*609-43_*609-42insTG
ENST00000696195.1:n.3822-43_3822-42insTG (F12)
ENST00000696200.1:n.1122-43_1122-42insTG (F12)
ENST00000696201.1:c.1019-43_1019-42insTG (F12)	ENSP00000512482.1:n.1019-43_1019-42insTG
ENST00000253496.4:c.1019-43_1019-42insTG (F12) MANE Select	ENSP00000253496.3:n.1019-43_1019-42insTG
ENST00000253496.3:c.1019-43_1019-42insTG (F12)	ENSP00000253496.3:n.1019-43_1019-42insTG
ENST00000502598.5:c.-45+607_-45+608insAC (GRK6)	ENSP00000422873.1:n.-45+607_-45+608insAC
ENST00000502854.5:n.278-43_278-42insTG (F12)
ENST00000503736.1:n.391-43_391-42insTG (F12)
ENST00000510358.5:n.340_341insTG (F12)
NM_000505.3:c.1019-43_1019-42insTG , LRG_145t1:c.1019-43_1019-42insTG (F12)	NP_000496.2:n.1019-43_1019-42insTG
XM_011534461.1:c.1019-43_1019-42insTG (F12)	XP_011532763.1:n.1019-43_1019-42insTG
XM_011534462.1:c.683-43_683-42insTG (F12)	XP_011532764.1:n.683-43_683-42insTG
XM_011534462.2:c.683-43_683-42insTG (F12)	XP_011532764.1:n.683-43_683-42insTG
XM_017009773.2:c.1416+7059_1416+7060insAC (SLC34A1)	XP_016865262.1:n.1416+7059_1416+7060insAC
NM_000505.4:c.1019-43_1019-42insTG (F12) MANE Select	NP_000496.2:n.1019-43_1019-42insTG