Canonical Allele Identifier: CA348406204

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186330C>A (hg19) ; chr2:g.127428754C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428754C>A , CM000664.2:g.127428754C>A	GRCh38
NC_000002.11:g.128186330C>A , CM000664.1:g.128186330C>A	GRCh37
NC_000002.10:g.127902800C>A	NCBI36
NG_016323.1:g.15335C>A , LRG_599:g.15335C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1194C>A MANE Select	ENSP00000234071.4:p.Cys398Ter
ENST00000234071.7:c.1194C>A	ENSP00000234071.3:p.Cys398Ter
ENST00000402125.2:c.518C>A
ENST00000409048.1:c.1296C>A	ENSP00000386679.1:p.Cys432Ter
NM_000312.3:c.1194C>A , LRG_599t1:c.1194C>A	NP_000303.1:p.Cys398Ter
XM_005263715.3:c.1377C>A	XP_005263772.1:p.Cys459Ter
XM_005263716.3:c.1359C>A	XP_005263773.1:p.Cys453Ter
XM_005263717.3:c.1257C>A	XP_005263774.1:p.Cys419Ter
XR_923313.1:n.1332-490G>T
XM_005263717.4:c.1257C>A	XP_005263774.1:p.Cys419Ter
XM_017004505.1:c.1437C>A	XP_016859994.1:p.Cys479Ter
XM_024453002.1:c.1539C>A	XP_024308770.1:p.Cys513Ter
XM_024453003.1:c.1479C>A	XP_024308771.1:p.Cys493Ter
XM_024453004.1:c.1377C>A	XP_024308772.1:p.Cys459Ter
XM_024453005.1:c.1359C>A	XP_024308773.1:p.Cys453Ter
XM_024453006.1:c.1296C>A	XP_024308774.1:p.Cys432Ter
XR_001739705.1:n.3607-490G>T
XR_923313.2:n.4043-490G>T
NM_000312.4:c.1194C>A MANE Select	NP_000303.1:p.Cys398Ter
NM_001375602.1:c.1377C>A	NP_001362531.1:p.Cys459Ter
NM_001375603.1:c.1359C>A	NP_001362532.1:p.Cys453Ter
NM_001375604.1:c.1257C>A	NP_001362533.1:p.Cys419Ter
NM_001375605.1:c.1296C>A	NP_001362534.1:p.Cys432Ter
NM_001375606.1:c.1362C>A	NP_001362535.1:p.Cys454Ter
NM_001375607.1:c.1380C>A	NP_001362536.1:p.Cys460Ter
NM_001375608.1:c.1137C>A	NP_001362537.1:p.Cys379Ter
NM_001375609.1:c.1170C>A	NP_001362538.1:p.Cys390Ter
NM_001375610.1:c.1188C>A	NP_001362539.1:p.Cys396Ter
NM_001375611.1:c.1194C>A	NP_001362540.1:p.Cys398Ter
NM_001375613.1:c.1194C>A	NP_001362542.1:p.Cys398Ter