Canonical Allele Identifier: CA2676711577

Gene: F12 GRK6 SLC34A1

Linked Data

• gnomAD v4: 5-177404439-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404439T>G , CM000667.2:g.177404439T>G	GRCh38
NC_000005.9:g.176831440T>G , CM000667.1:g.176831440T>G	GRCh37
NC_000005.8:g.176764046T>G	NCBI36
NG_007568.1:g.10138A>C , LRG_145:g.10138A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*467-26A>C (F12)	ENSP00000512476.1:n.*467-26A>C
ENST00000696193.1:c.*1171-26A>C (F12)	ENSP00000512477.1:n.*1171-26A>C
ENST00000696194.1:c.*391-26A>C (F12)	ENSP00000512478.1:n.*391-26A>C
ENST00000696195.1:n.3604-26A>C (F12)
ENST00000696200.1:n.904-26A>C (F12)
ENST00000696201.1:c.801-26A>C (F12)	ENSP00000512482.1:n.801-26A>C
ENST00000253496.4:c.801-26A>C (F12) MANE Select	ENSP00000253496.3:n.801-26A>C
ENST00000253496.3:c.801-26A>C (F12)	ENSP00000253496.3:n.801-26A>C
ENST00000502598.5:c.-45+913T>G (GRK6)	ENSP00000422873.1:n.-45+913T>G
ENST00000502854.5:n.34A>C (F12)
ENST00000503736.1:n.173-26A>C (F12)
ENST00000506296.5:c.-163T>G (GRK6)	ENSP00000421055.1:n.-163T>G
ENST00000510358.5:n.34A>C (F12)
NM_000505.3:c.801-26A>C , LRG_145t1:c.801-26A>C (F12)	NP_000496.2:n.801-26A>C
XM_011534461.1:c.801-26A>C (F12)	XP_011532763.1:n.801-26A>C
XM_011534462.1:c.465-26A>C (F12)	XP_011532764.1:n.465-26A>C
XM_011534462.2:c.465-26A>C (F12)	XP_011532764.1:n.465-26A>C
XM_017009773.2:c.1417-7325T>G (SLC34A1)	XP_016865262.1:n.1417-7325T>G
NM_000505.4:c.801-26A>C (F12) MANE Select	NP_000496.2:n.801-26A>C