Canonical Allele Identifier: CA1286883398

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426095T= , CM000664.2:g.127426095T=	GRCh38
NC_000002.11:g.128183671T= , CM000664.1:g.128183671T=	GRCh37
NC_000002.10:g.127900141T=	NCBI36
NG_016323.1:g.12676T= , LRG_599:g.12676T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.546T= MANE Select	ENSP00000234071.4:p.Pro182=
ENST00000234071.7:c.546T=	ENSP00000234071.3:p.Pro182=
ENST00000402125.2:c.121-2262T=
ENST00000409048.1:c.648T=	ENSP00000386679.1:p.Pro216=
ENST00000442644.5:c.489T=	ENSP00000411241.1:p.Pro163=
ENST00000464089.1:n.132T=
NM_000312.3:c.546T= , LRG_599t1:c.546T=	NP_000303.1:p.Pro182=
XM_005263715.3:c.729T=	XP_005263772.1:p.Pro243=
XM_005263716.3:c.711T=	XP_005263773.1:p.Pro237=
XM_005263717.3:c.609T=	XP_005263774.1:p.Pro203=
XM_005263717.4:c.609T=	XP_005263774.1:p.Pro203=
XM_017004505.1:c.789T=	XP_016859994.1:p.Pro263=
XM_024453002.1:c.891T=	XP_024308770.1:p.Pro297=
XM_024453003.1:c.831T=	XP_024308771.1:p.Pro277=
XM_024453004.1:c.729T=	XP_024308772.1:p.Pro243=
XM_024453005.1:c.711T=	XP_024308773.1:p.Pro237=
XM_024453006.1:c.648T=	XP_024308774.1:p.Pro216=
XR_923313.2:n.4490A=
NM_000312.4:c.546T= MANE Select	NP_000303.1:p.Pro182=
NM_001375602.1:c.729T=	NP_001362531.1:p.Pro243=
NM_001375603.1:c.711T=	NP_001362532.1:p.Pro237=
NM_001375604.1:c.609T=	NP_001362533.1:p.Pro203=
NM_001375605.1:c.648T=	NP_001362534.1:p.Pro216=
NM_001375606.1:c.714T=	NP_001362535.1:p.Pro238=
NM_001375607.1:c.732T=	NP_001362536.1:p.Pro244=
NM_001375608.1:c.489T=	NP_001362537.1:p.Pro163=
NM_001375609.1:c.522T=	NP_001362538.1:p.Pro174=
NM_001375610.1:c.540T=	NP_001362539.1:p.Pro180=
NM_001375611.1:c.546T=	NP_001362540.1:p.Pro182=
NM_001375613.1:c.546T=	NP_001362542.1:p.Pro182=