Canonical Allele Identifier: CA348401707
Gene: PROC HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.128183792A>C (hg19) chr2:g.127426216A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127426216A>C , CM000664.2:g.127426216A>C GRCh38
NC_000002.11:g.128183792A>C , CM000664.1:g.128183792A>C GRCh37
NC_000002.10:g.127900262A>C NCBI36
NG_016323.1:g.12797A>C , LRG_599:g.12797A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000234071.8:c.667A>C MANE Select ENSP00000234071.4:p.Ser223Arg
ENST00000234071.7:c.667A>C ENSP00000234071.3:p.Ser223Arg
ENST00000402125.2:c.121-2141A>C
ENST00000409048.1:c.769A>C ENSP00000386679.1:p.Ser257Arg
ENST00000464089.1:n.253A>C
NM_000312.3:c.667A>C , LRG_599t1:c.667A>C NP_000303.1:p.Ser223Arg
XM_005263715.3:c.850A>C XP_005263772.1:p.Ser284Arg
XM_005263716.3:c.832A>C XP_005263773.1:p.Ser278Arg
XM_005263717.3:c.730A>C XP_005263774.1:p.Ser244Arg
XM_005263717.4:c.730A>C XP_005263774.1:p.Ser244Arg
XM_017004505.1:c.910A>C XP_016859994.1:p.Ser304Arg
XM_024453002.1:c.1012A>C XP_024308770.1:p.Ser338Arg
XM_024453003.1:c.952A>C XP_024308771.1:p.Ser318Arg
XM_024453004.1:c.850A>C XP_024308772.1:p.Ser284Arg
XM_024453005.1:c.832A>C XP_024308773.1:p.Ser278Arg
XM_024453006.1:c.769A>C XP_024308774.1:p.Ser257Arg
XR_923313.2:n.4369T>G
NM_000312.4:c.667A>C MANE Select NP_000303.1:p.Ser223Arg
NM_001375602.1:c.850A>C NP_001362531.1:p.Ser284Arg
NM_001375603.1:c.832A>C NP_001362532.1:p.Ser278Arg
NM_001375604.1:c.730A>C NP_001362533.1:p.Ser244Arg
NM_001375605.1:c.769A>C NP_001362534.1:p.Ser257Arg
NM_001375606.1:c.835A>C NP_001362535.1:p.Ser279Arg
NM_001375607.1:c.853A>C NP_001362536.1:p.Ser285Arg
NM_001375608.1:c.610A>C NP_001362537.1:p.Ser204Arg
NM_001375609.1:c.643A>C NP_001362538.1:p.Ser215Arg
NM_001375610.1:c.661A>C NP_001362539.1:p.Ser221Arg
NM_001375611.1:c.667A>C NP_001362540.1:p.Ser223Arg
NM_001375613.1:c.667A>C NP_001362542.1:p.Ser223Arg
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