Canonical Allele Identifier: CA1286883436

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426176T= , CM000664.2:g.127426176T=	GRCh38
NC_000002.11:g.128183752T= , CM000664.1:g.128183752T=	GRCh37
NC_000002.10:g.127900222T=	NCBI36
NG_016323.1:g.12757T= , LRG_599:g.12757T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.627T= MANE Select	ENSP00000234071.4:p.Asp209=
ENST00000234071.7:c.627T=	ENSP00000234071.3:p.Asp209=
ENST00000402125.2:c.121-2181T=
ENST00000409048.1:c.729T=	ENSP00000386679.1:p.Asp243=
ENST00000464089.1:n.213T=
NM_000312.3:c.627T= , LRG_599t1:c.627T=	NP_000303.1:p.Asp209=
XM_005263715.3:c.810T=	XP_005263772.1:p.Asp270=
XM_005263716.3:c.792T=	XP_005263773.1:p.Asp264=
XM_005263717.3:c.690T=	XP_005263774.1:p.Asp230=
XM_005263717.4:c.690T=	XP_005263774.1:p.Asp230=
XM_017004505.1:c.870T=	XP_016859994.1:p.Asp290=
XM_024453002.1:c.972T=	XP_024308770.1:p.Asp324=
XM_024453003.1:c.912T=	XP_024308771.1:p.Asp304=
XM_024453004.1:c.810T=	XP_024308772.1:p.Asp270=
XM_024453005.1:c.792T=	XP_024308773.1:p.Asp264=
XM_024453006.1:c.729T=	XP_024308774.1:p.Asp243=
XR_923313.2:n.4409A=
NM_000312.4:c.627T= MANE Select	NP_000303.1:p.Asp209=
NM_001375602.1:c.810T=	NP_001362531.1:p.Asp270=
NM_001375603.1:c.792T=	NP_001362532.1:p.Asp264=
NM_001375604.1:c.690T=	NP_001362533.1:p.Asp230=
NM_001375605.1:c.729T=	NP_001362534.1:p.Asp243=
NM_001375606.1:c.795T=	NP_001362535.1:p.Asp265=
NM_001375607.1:c.813T=	NP_001362536.1:p.Asp271=
NM_001375608.1:c.570T=	NP_001362537.1:p.Asp190=
NM_001375609.1:c.603T=	NP_001362538.1:p.Asp201=
NM_001375610.1:c.621T=	NP_001362539.1:p.Asp207=
NM_001375611.1:c.627T=	NP_001362540.1:p.Asp209=
NM_001375613.1:c.627T=	NP_001362542.1:p.Asp209=