Canonical Allele Identifier: CA428618275

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128183731A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426155A>G , CM000664.2:g.127426155A>G	GRCh38
NC_000002.11:g.128183731A>G , CM000664.1:g.128183731A>G	GRCh37
NC_000002.10:g.127900201A>G	NCBI36
NG_016323.1:g.12736A>G , LRG_599:g.12736A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.606A>G MANE Select	ENSP00000234071.4:p.Glu202=
ENST00000234071.7:c.606A>G	ENSP00000234071.3:p.Glu202=
ENST00000402125.2:c.121-2202A>G
ENST00000409048.1:c.708A>G	ENSP00000386679.1:p.Glu236=
ENST00000464089.1:n.192A>G
NM_000312.3:c.606A>G , LRG_599t1:c.606A>G	NP_000303.1:p.Glu202=
XM_005263715.3:c.789A>G	XP_005263772.1:p.Glu263=
XM_005263716.3:c.771A>G	XP_005263773.1:p.Glu257=
XM_005263717.3:c.669A>G	XP_005263774.1:p.Glu223=
XM_005263717.4:c.669A>G	XP_005263774.1:p.Glu223=
XM_017004505.1:c.849A>G	XP_016859994.1:p.Glu283=
XM_024453002.1:c.951A>G	XP_024308770.1:p.Glu317=
XM_024453003.1:c.891A>G	XP_024308771.1:p.Glu297=
XM_024453004.1:c.789A>G	XP_024308772.1:p.Glu263=
XM_024453005.1:c.771A>G	XP_024308773.1:p.Glu257=
XM_024453006.1:c.708A>G	XP_024308774.1:p.Glu236=
XR_923313.2:n.4430T>C
NM_000312.4:c.606A>G MANE Select	NP_000303.1:p.Glu202=
NM_001375602.1:c.789A>G	NP_001362531.1:p.Glu263=
NM_001375603.1:c.771A>G	NP_001362532.1:p.Glu257=
NM_001375604.1:c.669A>G	NP_001362533.1:p.Glu223=
NM_001375605.1:c.708A>G	NP_001362534.1:p.Glu236=
NM_001375606.1:c.774A>G	NP_001362535.1:p.Glu258=
NM_001375607.1:c.792A>G	NP_001362536.1:p.Glu264=
NM_001375608.1:c.549A>G	NP_001362537.1:p.Glu183=
NM_001375609.1:c.582A>G	NP_001362538.1:p.Glu194=
NM_001375610.1:c.600A>G	NP_001362539.1:p.Glu200=
NM_001375611.1:c.606A>G	NP_001362540.1:p.Glu202=
NM_001375613.1:c.606A>G	NP_001362542.1:p.Glu202=