Canonical Allele Identifier: CA362329448

Gene: F12 GRK6 SLC34A1

Linked Data

• MyVariant Identifiers: chr5:g.176831642C>T (hg19) ; chr5:g.177404641C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404641C>T , CM000667.2:g.177404641C>T	GRCh38
NC_000005.9:g.176831642C>T , CM000667.1:g.176831642C>T	GRCh37
NC_000005.8:g.176764248C>T	NCBI36
NG_007568.1:g.9936G>A , LRG_145:g.9936G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*324G>A (F12)	ENSP00000512476.1:n.*324G>A
ENST00000696193.1:c.*1028G>A (F12)	ENSP00000512477.1:n.*1028G>A
ENST00000696194.1:c.*248G>A (F12)	ENSP00000512478.1:n.*248G>A
ENST00000696195.1:n.3461G>A (F12)
ENST00000696200.1:n.761G>A (F12)
ENST00000696201.1:c.658G>A (F12)	ENSP00000512482.1:p.Gly220Ser
ENST00000253496.4:c.658G>A (F12) MANE Select	ENSP00000253496.3:p.Gly220Ser
ENST00000253496.3:c.658G>A (F12)	ENSP00000253496.3:p.Gly220Ser
ENST00000502598.5:c.-45+1115C>T (GRK6)	ENSP00000422873.1:n.-45+1115C>T
ENST00000503736.1:n.172+169G>A (F12)
ENST00000506296.5:c.-45+84C>T (GRK6)	ENSP00000421055.1:n.-45+84C>T
NM_000505.3:c.658G>A , LRG_145t1:c.658G>A (F12)	NP_000496.2:p.Gly220Ser
XM_011534461.1:c.658G>A (F12)	XP_011532763.1:p.Gly220Ser
XM_011534462.1:c.322G>A (F12)	XP_011532764.1:p.Gly108Ser
XM_011534462.2:c.322G>A (F12)	XP_011532764.1:p.Gly108Ser
XM_017009773.2:c.1417-7123C>T (SLC34A1)	XP_016865262.1:n.1417-7123C>T
NM_000505.4:c.658G>A (F12) MANE Select	NP_000496.2:p.Gly220Ser