Canonical Allele Identifier: CA348401677

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128183787G>T (hg19) ; chr2:g.127426211G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426211G>T , CM000664.2:g.127426211G>T	GRCh38
NC_000002.11:g.128183787G>T , CM000664.1:g.128183787G>T	GRCh37
NC_000002.10:g.127900257G>T	NCBI36
NG_016323.1:g.12792G>T , LRG_599:g.12792G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.662G>T MANE Select	ENSP00000234071.4:p.Gly221Val
ENST00000234071.7:c.662G>T	ENSP00000234071.3:p.Gly221Val
ENST00000402125.2:c.121-2146G>T
ENST00000409048.1:c.764G>T	ENSP00000386679.1:p.Gly255Val
ENST00000464089.1:n.248G>T
NM_000312.3:c.662G>T , LRG_599t1:c.662G>T	NP_000303.1:p.Gly221Val
XM_005263715.3:c.845G>T	XP_005263772.1:p.Gly282Val
XM_005263716.3:c.827G>T	XP_005263773.1:p.Gly276Val
XM_005263717.3:c.725G>T	XP_005263774.1:p.Gly242Val
XM_005263717.4:c.725G>T	XP_005263774.1:p.Gly242Val
XM_017004505.1:c.905G>T	XP_016859994.1:p.Gly302Val
XM_024453002.1:c.1007G>T	XP_024308770.1:p.Gly336Val
XM_024453003.1:c.947G>T	XP_024308771.1:p.Gly316Val
XM_024453004.1:c.845G>T	XP_024308772.1:p.Gly282Val
XM_024453005.1:c.827G>T	XP_024308773.1:p.Gly276Val
XM_024453006.1:c.764G>T	XP_024308774.1:p.Gly255Val
XR_923313.2:n.4374C>A
NM_000312.4:c.662G>T MANE Select	NP_000303.1:p.Gly221Val
NM_001375602.1:c.845G>T	NP_001362531.1:p.Gly282Val
NM_001375603.1:c.827G>T	NP_001362532.1:p.Gly276Val
NM_001375604.1:c.725G>T	NP_001362533.1:p.Gly242Val
NM_001375605.1:c.764G>T	NP_001362534.1:p.Gly255Val
NM_001375606.1:c.830G>T	NP_001362535.1:p.Gly277Val
NM_001375607.1:c.848G>T	NP_001362536.1:p.Gly283Val
NM_001375608.1:c.605G>T	NP_001362537.1:p.Gly202Val
NM_001375609.1:c.638G>T	NP_001362538.1:p.Gly213Val
NM_001375610.1:c.656G>T	NP_001362539.1:p.Gly219Val
NM_001375611.1:c.662G>T	NP_001362540.1:p.Gly221Val
NM_001375613.1:c.662G>T	NP_001362542.1:p.Gly221Val