Canonical Allele Identifier: CA362329034

Gene: F12 GRK6 SLC34A1

Linked Data

• MyVariant Identifiers: chr5:g.176831526C>T (hg19) ; chr5:g.177404525C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404525C>T , CM000667.2:g.177404525C>T	GRCh38
NC_000005.9:g.176831526C>T , CM000667.1:g.176831526C>T	GRCh37
NC_000005.8:g.176764132C>T	NCBI36
NG_007568.1:g.10052G>A , LRG_145:g.10052G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*440G>A (F12)	ENSP00000512476.1:n.*440G>A
ENST00000696193.1:c.*1144G>A (F12)	ENSP00000512477.1:n.*1144G>A
ENST00000696194.1:c.*364G>A (F12)	ENSP00000512478.1:n.*364G>A
ENST00000696195.1:n.3577G>A (F12)
ENST00000696200.1:n.877G>A (F12)
ENST00000696201.1:c.774G>A (F12)	ENSP00000512482.1:p.Trp258Ter
ENST00000253496.4:c.774G>A (F12) MANE Select	ENSP00000253496.3:p.Trp258Ter
ENST00000253496.3:c.774G>A (F12)	ENSP00000253496.3:p.Trp258Ter
ENST00000502598.5:c.-45+999C>T (GRK6)	ENSP00000422873.1:n.-45+999C>T
ENST00000503736.1:n.173-112G>A (F12)
ENST00000506296.5:c.-77C>T (GRK6)	ENSP00000421055.1:n.-77C>T
NM_000505.3:c.774G>A , LRG_145t1:c.774G>A (F12)	NP_000496.2:p.Trp258Ter
XM_011534461.1:c.774G>A (F12)	XP_011532763.1:p.Trp258Ter
XM_011534462.1:c.438G>A (F12)	XP_011532764.1:p.Trp146Ter
XM_011534462.2:c.438G>A (F12)	XP_011532764.1:p.Trp146Ter
XM_017009773.2:c.1417-7239C>T (SLC34A1)	XP_016865262.1:n.1417-7239C>T
NM_000505.4:c.774G>A (F12) MANE Select	NP_000496.2:p.Trp258Ter