Canonical Allele Identifier: CA348406208

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186331G>T (hg19) ; chr2:g.127428755G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428755G>T , CM000664.2:g.127428755G>T	GRCh38
NC_000002.11:g.128186331G>T , CM000664.1:g.128186331G>T	GRCh37
NC_000002.10:g.127902801G>T	NCBI36
NG_016323.1:g.15336G>T , LRG_599:g.15336G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1195G>T MANE Select	ENSP00000234071.4:p.Glu399Ter
ENST00000234071.7:c.1195G>T	ENSP00000234071.3:p.Glu399Ter
ENST00000402125.2:c.519G>T
ENST00000409048.1:c.1297G>T	ENSP00000386679.1:p.Glu433Ter
NM_000312.3:c.1195G>T , LRG_599t1:c.1195G>T	NP_000303.1:p.Glu399Ter
XM_005263715.3:c.1378G>T	XP_005263772.1:p.Glu460Ter
XM_005263716.3:c.1360G>T	XP_005263773.1:p.Glu454Ter
XM_005263717.3:c.1258G>T	XP_005263774.1:p.Glu420Ter
XR_923313.1:n.1332-491C>A
XM_005263717.4:c.1258G>T	XP_005263774.1:p.Glu420Ter
XM_017004505.1:c.1438G>T	XP_016859994.1:p.Glu480Ter
XM_024453002.1:c.1540G>T	XP_024308770.1:p.Glu514Ter
XM_024453003.1:c.1480G>T	XP_024308771.1:p.Glu494Ter
XM_024453004.1:c.1378G>T	XP_024308772.1:p.Glu460Ter
XM_024453005.1:c.1360G>T	XP_024308773.1:p.Glu454Ter
XM_024453006.1:c.1297G>T	XP_024308774.1:p.Glu433Ter
XR_001739705.1:n.3607-491C>A
XR_923313.2:n.4043-491C>A
NM_000312.4:c.1195G>T MANE Select	NP_000303.1:p.Glu399Ter
NM_001375602.1:c.1378G>T	NP_001362531.1:p.Glu460Ter
NM_001375603.1:c.1360G>T	NP_001362532.1:p.Glu454Ter
NM_001375604.1:c.1258G>T	NP_001362533.1:p.Glu420Ter
NM_001375605.1:c.1297G>T	NP_001362534.1:p.Glu433Ter
NM_001375606.1:c.1363G>T	NP_001362535.1:p.Glu455Ter
NM_001375607.1:c.1381G>T	NP_001362536.1:p.Glu461Ter
NM_001375608.1:c.1138G>T	NP_001362537.1:p.Glu380Ter
NM_001375609.1:c.1171G>T	NP_001362538.1:p.Glu391Ter
NM_001375610.1:c.1189G>T	NP_001362539.1:p.Glu397Ter
NM_001375611.1:c.1195G>T	NP_001362540.1:p.Glu399Ter
NM_001375613.1:c.1195G>T	NP_001362542.1:p.Glu399Ter