Canonical Allele Identifier: CA348401789
Gene: PROC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127426223G>T , CM000664.2:g.127426223G>T GRCh38
NC_000002.11:g.128183799G>T , CM000664.1:g.128183799G>T GRCh37
NC_000002.10:g.127900269G>T NCBI36
NG_016323.1:g.12804G>T , LRG_599:g.12804G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.674G>T MANE Select ENSP00000234071.4:p.Trp225Leu
ENST00000234071.7:c.674G>T ENSP00000234071.3:p.Trp225Leu
ENST00000402125.2:c.121-2134G>T
ENST00000409048.1:c.776G>T ENSP00000386679.1:p.Trp259Leu
ENST00000464089.1:n.260G>T
NM_000312.3:c.674G>T , LRG_599t1:c.674G>T NP_000303.1:p.Trp225Leu
XM_005263715.3:c.857G>T XP_005263772.1:p.Trp286Leu
XM_005263716.3:c.839G>T XP_005263773.1:p.Trp280Leu
XM_005263717.3:c.737G>T XP_005263774.1:p.Trp246Leu
XM_005263717.4:c.737G>T XP_005263774.1:p.Trp246Leu
XM_017004505.1:c.917G>T XP_016859994.1:p.Trp306Leu
XM_024453002.1:c.1019G>T XP_024308770.1:p.Trp340Leu
XM_024453003.1:c.959G>T XP_024308771.1:p.Trp320Leu
XM_024453004.1:c.857G>T XP_024308772.1:p.Trp286Leu
XM_024453005.1:c.839G>T XP_024308773.1:p.Trp280Leu
XM_024453006.1:c.776G>T XP_024308774.1:p.Trp259Leu
XR_923313.2:n.4362C>A
NM_000312.4:c.674G>T MANE Select NP_000303.1:p.Trp225Leu
NM_001375602.1:c.857G>T NP_001362531.1:p.Trp286Leu
NM_001375603.1:c.839G>T NP_001362532.1:p.Trp280Leu
NM_001375604.1:c.737G>T NP_001362533.1:p.Trp246Leu
NM_001375605.1:c.776G>T NP_001362534.1:p.Trp259Leu
NM_001375606.1:c.842G>T NP_001362535.1:p.Trp281Leu
NM_001375607.1:c.860G>T NP_001362536.1:p.Trp287Leu
NM_001375608.1:c.617G>T NP_001362537.1:p.Trp206Leu
NM_001375609.1:c.650G>T NP_001362538.1:p.Trp217Leu
NM_001375610.1:c.668G>T NP_001362539.1:p.Trp223Leu
NM_001375611.1:c.674G>T NP_001362540.1:p.Trp225Leu
NM_001375613.1:c.674G>T NP_001362542.1:p.Trp225Leu