Canonical Allele Identifier: CA348404569

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186010A>C (hg19) ; chr2:g.127428434A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428434A>C , CM000664.2:g.127428434A>C	GRCh38
NC_000002.11:g.128186010A>C , CM000664.1:g.128186010A>C	GRCh37
NC_000002.10:g.127902480A>C	NCBI36
NG_016323.1:g.15015A>C , LRG_599:g.15015A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.874A>C MANE Select	ENSP00000234071.4:p.Ser292Arg
ENST00000234071.7:c.874A>C	ENSP00000234071.3:p.Ser292Arg
ENST00000402125.2:c.198A>C
ENST00000409048.1:c.976A>C	ENSP00000386679.1:p.Ser326Arg
NM_000312.3:c.874A>C , LRG_599t1:c.874A>C	NP_000303.1:p.Ser292Arg
XM_005263715.3:c.1057A>C	XP_005263772.1:p.Ser353Arg
XM_005263716.3:c.1039A>C	XP_005263773.1:p.Ser347Arg
XM_005263717.3:c.937A>C	XP_005263774.1:p.Ser313Arg
XR_923313.1:n.1332-170T>G
XM_005263717.4:c.937A>C	XP_005263774.1:p.Ser313Arg
XM_017004505.1:c.1117A>C	XP_016859994.1:p.Ser373Arg
XM_024453002.1:c.1219A>C	XP_024308770.1:p.Ser407Arg
XM_024453003.1:c.1159A>C	XP_024308771.1:p.Ser387Arg
XM_024453004.1:c.1057A>C	XP_024308772.1:p.Ser353Arg
XM_024453005.1:c.1039A>C	XP_024308773.1:p.Ser347Arg
XM_024453006.1:c.976A>C	XP_024308774.1:p.Ser326Arg
XR_001739705.1:n.3607-170T>G
XR_923313.2:n.4043-170T>G
NM_000312.4:c.874A>C MANE Select	NP_000303.1:p.Ser292Arg
NM_001375602.1:c.1057A>C	NP_001362531.1:p.Ser353Arg
NM_001375603.1:c.1039A>C	NP_001362532.1:p.Ser347Arg
NM_001375604.1:c.937A>C	NP_001362533.1:p.Ser313Arg
NM_001375605.1:c.976A>C	NP_001362534.1:p.Ser326Arg
NM_001375606.1:c.1042A>C	NP_001362535.1:p.Ser348Arg
NM_001375607.1:c.1060A>C	NP_001362536.1:p.Ser354Arg
NM_001375608.1:c.817A>C	NP_001362537.1:p.Ser273Arg
NM_001375609.1:c.850A>C	NP_001362538.1:p.Ser284Arg
NM_001375610.1:c.868A>C	NP_001362539.1:p.Ser290Arg
NM_001375611.1:c.874A>C	NP_001362540.1:p.Ser292Arg
NM_001375613.1:c.874A>C	NP_001362542.1:p.Ser292Arg