Canonical Allele Identifier: CA348401414
Gene: PROC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127426163A>G , CM000664.2:g.127426163A>G GRCh38
NC_000002.11:g.128183739A>G , CM000664.1:g.128183739A>G GRCh37
NC_000002.10:g.127900209A>G NCBI36
NG_016323.1:g.12744A>G , LRG_599:g.12744A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.614A>G MANE Select ENSP00000234071.4:p.Glu205Gly
ENST00000234071.7:c.614A>G ENSP00000234071.3:p.Glu205Gly
ENST00000402125.2:c.121-2194A>G
ENST00000409048.1:c.716A>G ENSP00000386679.1:p.Glu239Gly
ENST00000464089.1:n.200A>G
NM_000312.3:c.614A>G , LRG_599t1:c.614A>G NP_000303.1:p.Glu205Gly
XM_005263715.3:c.797A>G XP_005263772.1:p.Glu266Gly
XM_005263716.3:c.779A>G XP_005263773.1:p.Glu260Gly
XM_005263717.3:c.677A>G XP_005263774.1:p.Glu226Gly
XM_005263717.4:c.677A>G XP_005263774.1:p.Glu226Gly
XM_017004505.1:c.857A>G XP_016859994.1:p.Glu286Gly
XM_024453002.1:c.959A>G XP_024308770.1:p.Glu320Gly
XM_024453003.1:c.899A>G XP_024308771.1:p.Glu300Gly
XM_024453004.1:c.797A>G XP_024308772.1:p.Glu266Gly
XM_024453005.1:c.779A>G XP_024308773.1:p.Glu260Gly
XM_024453006.1:c.716A>G XP_024308774.1:p.Glu239Gly
XR_923313.2:n.4422T>C
NM_000312.4:c.614A>G MANE Select NP_000303.1:p.Glu205Gly
NM_001375602.1:c.797A>G NP_001362531.1:p.Glu266Gly
NM_001375603.1:c.779A>G NP_001362532.1:p.Glu260Gly
NM_001375604.1:c.677A>G NP_001362533.1:p.Glu226Gly
NM_001375605.1:c.716A>G NP_001362534.1:p.Glu239Gly
NM_001375606.1:c.782A>G NP_001362535.1:p.Glu261Gly
NM_001375607.1:c.800A>G NP_001362536.1:p.Glu267Gly
NM_001375608.1:c.557A>G NP_001362537.1:p.Glu186Gly
NM_001375609.1:c.590A>G NP_001362538.1:p.Glu197Gly
NM_001375610.1:c.608A>G NP_001362539.1:p.Glu203Gly
NM_001375611.1:c.614A>G NP_001362540.1:p.Glu205Gly
NM_001375613.1:c.614A>G NP_001362542.1:p.Glu205Gly