Canonical Allele Identifier: CA1286883397

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426093C= , CM000664.2:g.127426093C=	GRCh38
NC_000002.11:g.128183669C= , CM000664.1:g.128183669C=	GRCh37
NC_000002.10:g.127900139C=	NCBI36
NG_016323.1:g.12674C= , LRG_599:g.12674C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.544C= MANE Select	ENSP00000234071.4:p.Pro182=
ENST00000234071.7:c.544C=	ENSP00000234071.3:p.Pro182=
ENST00000402125.2:c.121-2264C=
ENST00000409048.1:c.646C=	ENSP00000386679.1:p.Pro216=
ENST00000442644.5:c.487C=	ENSP00000411241.1:p.Pro163=
ENST00000464089.1:n.130C=
NM_000312.3:c.544C= , LRG_599t1:c.544C=	NP_000303.1:p.Pro182=
XM_005263715.3:c.727C=	XP_005263772.1:p.Pro243=
XM_005263716.3:c.709C=	XP_005263773.1:p.Pro237=
XM_005263717.3:c.607C=	XP_005263774.1:p.Pro203=
XM_005263717.4:c.607C=	XP_005263774.1:p.Pro203=
XM_017004505.1:c.787C=	XP_016859994.1:p.Pro263=
XM_024453002.1:c.889C=	XP_024308770.1:p.Pro297=
XM_024453003.1:c.829C=	XP_024308771.1:p.Pro277=
XM_024453004.1:c.727C=	XP_024308772.1:p.Pro243=
XM_024453005.1:c.709C=	XP_024308773.1:p.Pro237=
XM_024453006.1:c.646C=	XP_024308774.1:p.Pro216=
XR_923313.2:n.4492G=
NM_000312.4:c.544C= MANE Select	NP_000303.1:p.Pro182=
NM_001375602.1:c.727C=	NP_001362531.1:p.Pro243=
NM_001375603.1:c.709C=	NP_001362532.1:p.Pro237=
NM_001375604.1:c.607C=	NP_001362533.1:p.Pro203=
NM_001375605.1:c.646C=	NP_001362534.1:p.Pro216=
NM_001375606.1:c.712C=	NP_001362535.1:p.Pro238=
NM_001375607.1:c.730C=	NP_001362536.1:p.Pro244=
NM_001375608.1:c.487C=	NP_001362537.1:p.Pro163=
NM_001375609.1:c.520C=	NP_001362538.1:p.Pro174=
NM_001375610.1:c.538C=	NP_001362539.1:p.Pro180=
NM_001375611.1:c.544C=	NP_001362540.1:p.Pro182=
NM_001375613.1:c.544C=	NP_001362542.1:p.Pro182=