Canonical Allele Identifier: CA348401679

Gene: PROC

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.662G>A MANE Select	ENSP00000234071.4:p.Gly221Glu
ENST00000234071.7:c.662G>A	ENSP00000234071.3:p.Gly221Glu
ENST00000402125.2:c.121-2146G>A
ENST00000409048.1:c.764G>A	ENSP00000386679.1:p.Gly255Glu
ENST00000464089.1:n.248G>A
NM_000312.3:c.662G>A , LRG_599t1:c.662G>A	NP_000303.1:p.Gly221Glu
XM_005263715.3:c.845G>A	XP_005263772.1:p.Gly282Glu
XM_005263716.3:c.827G>A	XP_005263773.1:p.Gly276Glu
XM_005263717.3:c.725G>A	XP_005263774.1:p.Gly242Glu
XM_005263717.4:c.725G>A	XP_005263774.1:p.Gly242Glu
XM_017004505.1:c.905G>A	XP_016859994.1:p.Gly302Glu
XM_024453002.1:c.1007G>A	XP_024308770.1:p.Gly336Glu
XM_024453003.1:c.947G>A	XP_024308771.1:p.Gly316Glu
XM_024453004.1:c.845G>A	XP_024308772.1:p.Gly282Glu
XM_024453005.1:c.827G>A	XP_024308773.1:p.Gly276Glu
XM_024453006.1:c.764G>A	XP_024308774.1:p.Gly255Glu
XR_923313.2:n.4374C>T
NM_000312.4:c.662G>A MANE Select	NP_000303.1:p.Gly221Glu
NM_001375602.1:c.845G>A	NP_001362531.1:p.Gly282Glu
NM_001375603.1:c.827G>A	NP_001362532.1:p.Gly276Glu
NM_001375604.1:c.725G>A	NP_001362533.1:p.Gly242Glu
NM_001375605.1:c.764G>A	NP_001362534.1:p.Gly255Glu
NM_001375606.1:c.830G>A	NP_001362535.1:p.Gly277Glu
NM_001375607.1:c.848G>A	NP_001362536.1:p.Gly283Glu
NM_001375608.1:c.605G>A	NP_001362537.1:p.Gly202Glu
NM_001375609.1:c.638G>A	NP_001362538.1:p.Gly213Glu
NM_001375610.1:c.656G>A	NP_001362539.1:p.Gly219Glu
NM_001375611.1:c.662G>A	NP_001362540.1:p.Gly221Glu
NM_001375613.1:c.662G>A	NP_001362542.1:p.Gly221Glu