Canonical Allele Identifier: CA348401227
Gene: PROC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127426134T>A , CM000664.2:g.127426134T>A GRCh38
NC_000002.11:g.128183710T>A , CM000664.1:g.128183710T>A GRCh37
NC_000002.10:g.127900180T>A NCBI36
NG_016323.1:g.12715T>A , LRG_599:g.12715T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.585T>A MANE Select ENSP00000234071.4:p.Ser195Arg
ENST00000234071.7:c.585T>A ENSP00000234071.3:p.Ser195Arg
ENST00000402125.2:c.121-2223T>A
ENST00000409048.1:c.687T>A ENSP00000386679.1:p.Ser229Arg
ENST00000464089.1:n.171T>A
NM_000312.3:c.585T>A , LRG_599t1:c.585T>A NP_000303.1:p.Ser195Arg
XM_005263715.3:c.768T>A XP_005263772.1:p.Ser256Arg
XM_005263716.3:c.750T>A XP_005263773.1:p.Ser250Arg
XM_005263717.3:c.648T>A XP_005263774.1:p.Ser216Arg
XM_005263717.4:c.648T>A XP_005263774.1:p.Ser216Arg
XM_017004505.1:c.828T>A XP_016859994.1:p.Ser276Arg
XM_024453002.1:c.930T>A XP_024308770.1:p.Ser310Arg
XM_024453003.1:c.870T>A XP_024308771.1:p.Ser290Arg
XM_024453004.1:c.768T>A XP_024308772.1:p.Ser256Arg
XM_024453005.1:c.750T>A XP_024308773.1:p.Ser250Arg
XM_024453006.1:c.687T>A XP_024308774.1:p.Ser229Arg
XR_923313.2:n.4451A>T
NM_000312.4:c.585T>A MANE Select NP_000303.1:p.Ser195Arg
NM_001375602.1:c.768T>A NP_001362531.1:p.Ser256Arg
NM_001375603.1:c.750T>A NP_001362532.1:p.Ser250Arg
NM_001375604.1:c.648T>A NP_001362533.1:p.Ser216Arg
NM_001375605.1:c.687T>A NP_001362534.1:p.Ser229Arg
NM_001375606.1:c.753T>A NP_001362535.1:p.Ser251Arg
NM_001375607.1:c.771T>A NP_001362536.1:p.Ser257Arg
NM_001375608.1:c.528T>A NP_001362537.1:p.Ser176Arg
NM_001375609.1:c.561T>A NP_001362538.1:p.Ser187Arg
NM_001375610.1:c.579T>A NP_001362539.1:p.Ser193Arg
NM_001375611.1:c.585T>A NP_001362540.1:p.Ser195Arg
NM_001375613.1:c.585T>A NP_001362542.1:p.Ser195Arg