Canonical Allele Identifier: CA348400972
Gene: PROC HGNC NCBI

Linked Data

dbSNP Id: rs1324719747

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127426093C>T , CM000664.2:g.127426093C>T GRCh38
NC_000002.11:g.128183669C>T , CM000664.1:g.128183669C>T GRCh37
NC_000002.10:g.127900139C>T NCBI36
NG_016323.1:g.12674C>T , LRG_599:g.12674C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.544C>T MANE Select ENSP00000234071.4:p.Pro182Ser
ENST00000234071.7:c.544C>T ENSP00000234071.3:p.Pro182Ser
ENST00000402125.2:c.121-2264C>T
ENST00000409048.1:c.646C>T ENSP00000386679.1:p.Pro216Ser
ENST00000442644.5:c.487C>T ENSP00000411241.1:p.Pro163Ser
ENST00000464089.1:n.130C>T
NM_000312.3:c.544C>T , LRG_599t1:c.544C>T NP_000303.1:p.Pro182Ser
XM_005263715.3:c.727C>T XP_005263772.1:p.Pro243Ser
XM_005263716.3:c.709C>T XP_005263773.1:p.Pro237Ser
XM_005263717.3:c.607C>T XP_005263774.1:p.Pro203Ser
XM_005263717.4:c.607C>T XP_005263774.1:p.Pro203Ser
XM_017004505.1:c.787C>T XP_016859994.1:p.Pro263Ser
XM_024453002.1:c.889C>T XP_024308770.1:p.Pro297Ser
XM_024453003.1:c.829C>T XP_024308771.1:p.Pro277Ser
XM_024453004.1:c.727C>T XP_024308772.1:p.Pro243Ser
XM_024453005.1:c.709C>T XP_024308773.1:p.Pro237Ser
XM_024453006.1:c.646C>T XP_024308774.1:p.Pro216Ser
XR_923313.2:n.4492G>A
NM_000312.4:c.544C>T MANE Select NP_000303.1:p.Pro182Ser
NM_001375602.1:c.727C>T NP_001362531.1:p.Pro243Ser
NM_001375603.1:c.709C>T NP_001362532.1:p.Pro237Ser
NM_001375604.1:c.607C>T NP_001362533.1:p.Pro203Ser
NM_001375605.1:c.646C>T NP_001362534.1:p.Pro216Ser
NM_001375606.1:c.712C>T NP_001362535.1:p.Pro238Ser
NM_001375607.1:c.730C>T NP_001362536.1:p.Pro244Ser
NM_001375608.1:c.487C>T NP_001362537.1:p.Pro163Ser
NM_001375609.1:c.520C>T NP_001362538.1:p.Pro174Ser
NM_001375610.1:c.538C>T NP_001362539.1:p.Pro180Ser
NM_001375611.1:c.544C>T NP_001362540.1:p.Pro182Ser
NM_001375613.1:c.544C>T NP_001362542.1:p.Pro182Ser