Canonical Allele Identifier: CA3581605

Gene: F12 GRK6 SLC34A1

Linked Data

• dbSNP Id: rs779717286
• ExAC: 5:176833056 G / C
• gnomAD v2: 5-176833056-G-C
• gnomAD v4: 5-177406055-G-C
• MyVariant Identifiers: chr5:g.176833056G>C (hg19) ; chr5:g.177406055G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177406055G>C , CM000667.2:g.177406055G>C	GRCh38
NC_000005.9:g.176833056G>C , CM000667.1:g.176833056G>C	GRCh37
NC_000005.8:g.176765662G>C	NCBI36
NG_007568.1:g.8522C>G , LRG_145:g.8522C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.122C>G (F12)	ENSP00000512476.1:p.Thr41Ser
ENST00000696193.1:c.*46C>G (F12)	ENSP00000512477.1:n.*46C>G
ENST00000696194.1:c.122C>G (F12)	ENSP00000512478.1:p.Thr41Ser
ENST00000696195.1:n.2479C>G (F12)
ENST00000696200.1:n.225C>G (F12)
ENST00000696201.1:c.122C>G (F12)	ENSP00000512482.1:p.Thr41Ser
ENST00000253496.4:c.122C>G (F12) MANE Select	ENSP00000253496.3:p.Thr41Ser
ENST00000253496.3:c.122C>G (F12)	ENSP00000253496.3:p.Thr41Ser
ENST00000502598.5:c.-45+2529G>C (GRK6)	ENSP00000422873.1:n.-45+2529G>C
ENST00000506296.5:c.-45+1498G>C (GRK6)	ENSP00000421055.1:n.-45+1498G>C
NM_000505.3:c.122C>G , LRG_145t1:c.122C>G (F12)	NP_000496.2:p.Thr41Ser
XM_011534461.1:c.122C>G (F12)	XP_011532763.1:p.Thr41Ser
XM_017009773.2:c.1417-5709G>C (SLC34A1)	XP_016865262.1:n.1417-5709G>C
NM_000505.4:c.122C>G (F12) MANE Select	NP_000496.2:p.Thr41Ser