Canonical Allele Identifier: CA362329138

Gene: F12 GRK6 SLC34A1

Linked Data

• MyVariant Identifiers: chr5:g.176831554T>G (hg19) ; chr5:g.177404553T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404553T>G , CM000667.2:g.177404553T>G	GRCh38
NC_000005.9:g.176831554T>G , CM000667.1:g.176831554T>G	GRCh37
NC_000005.8:g.176764160T>G	NCBI36
NG_007568.1:g.10024A>C , LRG_145:g.10024A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*412A>C (F12)	ENSP00000512476.1:n.*412A>C
ENST00000696193.1:c.*1116A>C (F12)	ENSP00000512477.1:n.*1116A>C
ENST00000696194.1:c.*336A>C (F12)	ENSP00000512478.1:n.*336A>C
ENST00000696195.1:n.3549A>C (F12)
ENST00000696200.1:n.849A>C (F12)
ENST00000696201.1:c.746A>C (F12)	ENSP00000512482.1:p.Asn249Thr
ENST00000253496.4:c.746A>C (F12) MANE Select	ENSP00000253496.3:p.Asn249Thr
ENST00000253496.3:c.746A>C (F12)	ENSP00000253496.3:p.Asn249Thr
ENST00000502598.5:c.-45+1027T>G (GRK6)	ENSP00000422873.1:n.-45+1027T>G
ENST00000503736.1:n.173-140A>C (F12)
ENST00000506296.5:c.-49T>G (GRK6)	ENSP00000421055.1:n.-49T>G
NM_000505.3:c.746A>C , LRG_145t1:c.746A>C (F12)	NP_000496.2:p.Asn249Thr
XM_011534461.1:c.746A>C (F12)	XP_011532763.1:p.Asn249Thr
XM_011534462.1:c.410A>C (F12)	XP_011532764.1:p.Asn137Thr
XM_011534462.2:c.410A>C (F12)	XP_011532764.1:p.Asn137Thr
XM_017009773.2:c.1417-7211T>G (SLC34A1)	XP_016865262.1:n.1417-7211T>G
NM_000505.4:c.746A>C (F12) MANE Select	NP_000496.2:p.Asn249Thr