Canonical Allele Identifier: CA447964991

Gene: F12 GRK6 SLC34A1

Linked Data

• gnomAD v4: 5-177404041-T-C
• MyVariant Identifiers: chr5:g.176831042T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404041T>C , CM000667.2:g.177404041T>C	GRCh38
NC_000005.9:g.176831042T>C , CM000667.1:g.176831042T>C	GRCh37
NC_000005.8:g.176763648T>C	NCBI36
NG_007568.1:g.10536A>G , LRG_145:g.10536A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696192.1:c.*734A>G (F12)	ENSP00000512476.1:n.*734A>G
ENST00000696193.1:c.*1455A>G (F12)	ENSP00000512477.1:n.*1455A>G
ENST00000696194.1:c.*658A>G (F12)	ENSP00000512478.1:n.*658A>G
ENST00000696195.1:n.3871A>G (F12)
ENST00000696200.1:n.1171A>G (F12)
ENST00000696201.1:c.1068A>G (F12)	ENSP00000512482.1:p.Pro356=
ENST00000253496.4:c.1068A>G (F12) MANE Select	ENSP00000253496.3:p.Pro356=
ENST00000253496.3:c.1068A>G (F12)	ENSP00000253496.3:p.Pro356=
ENST00000502598.5:c.-45+515T>C (GRK6)	ENSP00000422873.1:n.-45+515T>C
ENST00000502854.5:n.327A>G (F12)
ENST00000503736.1:n.440A>G (F12)
ENST00000510358.5:n.432A>G (F12)
NM_000505.3:c.1068A>G , LRG_145t1:c.1068A>G (F12)	NP_000496.2:p.Pro356=
XM_011534461.1:c.1068A>G (F12)	XP_011532763.1:p.Pro356=
XM_011534462.1:c.732A>G (F12)	XP_011532764.1:p.Pro244=
XM_011534462.2:c.732A>G (F12)	XP_011532764.1:p.Pro244=
XM_017009773.2:c.1416+6967T>C (SLC34A1)	XP_016865262.1:n.1416+6967T>C
NM_000505.4:c.1068A>G (F12) MANE Select	NP_000496.2:p.Pro356=