Canonical Allele Identifier: CA428618337
Gene: PROC HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.128183773G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127426197G>A , CM000664.2:g.127426197G>A GRCh38
NC_000002.11:g.128183773G>A , CM000664.1:g.128183773G>A GRCh37
NC_000002.10:g.127900243G>A NCBI36
NG_016323.1:g.12778G>A , LRG_599:g.12778G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.648G>A MANE Select ENSP00000234071.4:p.Lys216=
ENST00000234071.7:c.648G>A ENSP00000234071.3:p.Lys216=
ENST00000402125.2:c.121-2160G>A
ENST00000409048.1:c.750G>A ENSP00000386679.1:p.Lys250=
ENST00000464089.1:n.234G>A
NM_000312.3:c.648G>A , LRG_599t1:c.648G>A NP_000303.1:p.Lys216=
XM_005263715.3:c.831G>A XP_005263772.1:p.Lys277=
XM_005263716.3:c.813G>A XP_005263773.1:p.Lys271=
XM_005263717.3:c.711G>A XP_005263774.1:p.Lys237=
XM_005263717.4:c.711G>A XP_005263774.1:p.Lys237=
XM_017004505.1:c.891G>A XP_016859994.1:p.Lys297=
XM_024453002.1:c.993G>A XP_024308770.1:p.Lys331=
XM_024453003.1:c.933G>A XP_024308771.1:p.Lys311=
XM_024453004.1:c.831G>A XP_024308772.1:p.Lys277=
XM_024453005.1:c.813G>A XP_024308773.1:p.Lys271=
XM_024453006.1:c.750G>A XP_024308774.1:p.Lys250=
XR_923313.2:n.4388C>T
NM_000312.4:c.648G>A MANE Select NP_000303.1:p.Lys216=
NM_001375602.1:c.831G>A NP_001362531.1:p.Lys277=
NM_001375603.1:c.813G>A NP_001362532.1:p.Lys271=
NM_001375604.1:c.711G>A NP_001362533.1:p.Lys237=
NM_001375605.1:c.750G>A NP_001362534.1:p.Lys250=
NM_001375606.1:c.816G>A NP_001362535.1:p.Lys272=
NM_001375607.1:c.834G>A NP_001362536.1:p.Lys278=
NM_001375608.1:c.591G>A NP_001362537.1:p.Lys197=
NM_001375609.1:c.624G>A NP_001362538.1:p.Lys208=
NM_001375610.1:c.642G>A NP_001362539.1:p.Lys214=
NM_001375611.1:c.648G>A NP_001362540.1:p.Lys216=
NM_001375613.1:c.648G>A NP_001362542.1:p.Lys216=