Canonical Allele Identifier: CA1859394
Gene: PROC HGNC NCBI

Linked Data

dbSNP Id: rs762098236

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127426139T>C , CM000664.2:g.127426139T>C GRCh38
NC_000002.11:g.128183715T>C , CM000664.1:g.128183715T>C GRCh37
NC_000002.10:g.127900185T>C NCBI36
NG_016323.1:g.12720T>C , LRG_599:g.12720T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.590T>C MANE Select ENSP00000234071.4:p.Leu197Pro
ENST00000234071.7:c.590T>C ENSP00000234071.3:p.Leu197Pro
ENST00000402125.2:c.121-2218T>C
ENST00000409048.1:c.692T>C ENSP00000386679.1:p.Leu231Pro
ENST00000464089.1:n.176T>C
NM_000312.3:c.590T>C , LRG_599t1:c.590T>C NP_000303.1:p.Leu197Pro
XM_005263715.3:c.773T>C XP_005263772.1:p.Leu258Pro
XM_005263716.3:c.755T>C XP_005263773.1:p.Leu252Pro
XM_005263717.3:c.653T>C XP_005263774.1:p.Leu218Pro
XM_005263717.4:c.653T>C XP_005263774.1:p.Leu218Pro
XM_017004505.1:c.833T>C XP_016859994.1:p.Leu278Pro
XM_024453002.1:c.935T>C XP_024308770.1:p.Leu312Pro
XM_024453003.1:c.875T>C XP_024308771.1:p.Leu292Pro
XM_024453004.1:c.773T>C XP_024308772.1:p.Leu258Pro
XM_024453005.1:c.755T>C XP_024308773.1:p.Leu252Pro
XM_024453006.1:c.692T>C XP_024308774.1:p.Leu231Pro
XR_923313.2:n.4446A>G
NM_000312.4:c.590T>C MANE Select NP_000303.1:p.Leu197Pro
NM_001375602.1:c.773T>C NP_001362531.1:p.Leu258Pro
NM_001375603.1:c.755T>C NP_001362532.1:p.Leu252Pro
NM_001375604.1:c.653T>C NP_001362533.1:p.Leu218Pro
NM_001375605.1:c.692T>C NP_001362534.1:p.Leu231Pro
NM_001375606.1:c.758T>C NP_001362535.1:p.Leu253Pro
NM_001375607.1:c.776T>C NP_001362536.1:p.Leu259Pro
NM_001375608.1:c.533T>C NP_001362537.1:p.Leu178Pro
NM_001375609.1:c.566T>C NP_001362538.1:p.Leu189Pro
NM_001375610.1:c.584T>C NP_001362539.1:p.Leu195Pro
NM_001375611.1:c.590T>C NP_001362540.1:p.Leu197Pro
NM_001375613.1:c.590T>C NP_001362542.1:p.Leu197Pro