Canonical Allele Identifier: CA362335602

Gene: F12 GRK6 SLC34A1

Linked Data

• gnomAD v4: 5-177409490-C-G
• MyVariant Identifiers: chr5:g.176836491C>G (hg19) ; chr5:g.177409490C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177409490C>G , CM000667.2:g.177409490C>G	GRCh38
NC_000005.9:g.176836491C>G , CM000667.1:g.176836491C>G	GRCh37
NC_000005.8:g.176769097C>G	NCBI36
NG_007568.1:g.5087G>C , LRG_145:g.5087G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.38G>C (F12)	ENSP00000512476.1:p.Ser13Thr
ENST00000696193.1:c.38G>C (F12)	ENSP00000512477.1:p.Ser13Thr
ENST00000696194.1:c.38G>C (F12)	ENSP00000512478.1:p.Ser13Thr
ENST00000696195.1:n.86G>C (F12)
ENST00000696200.1:n.141G>C (F12)
ENST00000696201.1:c.38G>C (F12)	ENSP00000512482.1:p.Ser13Thr
ENST00000253496.4:c.38G>C (F12) MANE Select	ENSP00000253496.3:p.Ser13Thr
ENST00000253496.3:c.38G>C (F12)	ENSP00000253496.3:p.Ser13Thr
ENST00000502598.5:c.-45+5964C>G (GRK6)	ENSP00000422873.1:n.-45+5964C>G
ENST00000506296.5:c.-45+4933C>G (GRK6)	ENSP00000421055.1:n.-45+4933C>G
NM_000505.3:c.38G>C , LRG_145t1:c.38G>C (F12)	NP_000496.2:p.Ser13Thr
XM_011534461.1:c.38G>C (F12)	XP_011532763.1:p.Ser13Thr
XM_017009773.2:c.1417-2274C>G (SLC34A1)	XP_016865262.1:n.1417-2274C>G
NM_000505.4:c.38G>C (F12) MANE Select	NP_000496.2:p.Ser13Thr