Canonical Allele Identifier: CA428618335

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128183770G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426194G>C , CM000664.2:g.127426194G>C	GRCh38
NC_000002.11:g.128183770G>C , CM000664.1:g.128183770G>C	GRCh37
NC_000002.10:g.127900240G>C	NCBI36
NG_016323.1:g.12775G>C , LRG_599:g.12775G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.645G>C MANE Select	ENSP00000234071.4:p.Gly215=
ENST00000234071.7:c.645G>C	ENSP00000234071.3:p.Gly215=
ENST00000402125.2:c.121-2163G>C
ENST00000409048.1:c.747G>C	ENSP00000386679.1:p.Gly249=
ENST00000464089.1:n.231G>C
NM_000312.3:c.645G>C , LRG_599t1:c.645G>C	NP_000303.1:p.Gly215=
XM_005263715.3:c.828G>C	XP_005263772.1:p.Gly276=
XM_005263716.3:c.810G>C	XP_005263773.1:p.Gly270=
XM_005263717.3:c.708G>C	XP_005263774.1:p.Gly236=
XM_005263717.4:c.708G>C	XP_005263774.1:p.Gly236=
XM_017004505.1:c.888G>C	XP_016859994.1:p.Gly296=
XM_024453002.1:c.990G>C	XP_024308770.1:p.Gly330=
XM_024453003.1:c.930G>C	XP_024308771.1:p.Gly310=
XM_024453004.1:c.828G>C	XP_024308772.1:p.Gly276=
XM_024453005.1:c.810G>C	XP_024308773.1:p.Gly270=
XM_024453006.1:c.747G>C	XP_024308774.1:p.Gly249=
XR_923313.2:n.4391C>G
NM_000312.4:c.645G>C MANE Select	NP_000303.1:p.Gly215=
NM_001375602.1:c.828G>C	NP_001362531.1:p.Gly276=
NM_001375603.1:c.810G>C	NP_001362532.1:p.Gly270=
NM_001375604.1:c.708G>C	NP_001362533.1:p.Gly236=
NM_001375605.1:c.747G>C	NP_001362534.1:p.Gly249=
NM_001375606.1:c.813G>C	NP_001362535.1:p.Gly271=
NM_001375607.1:c.831G>C	NP_001362536.1:p.Gly277=
NM_001375608.1:c.588G>C	NP_001362537.1:p.Gly196=
NM_001375609.1:c.621G>C	NP_001362538.1:p.Gly207=
NM_001375610.1:c.639G>C	NP_001362539.1:p.Gly213=
NM_001375611.1:c.645G>C	NP_001362540.1:p.Gly215=
NM_001375613.1:c.645G>C	NP_001362542.1:p.Gly215=