Canonical Allele Identifier: CA1286883422

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426139T= , CM000664.2:g.127426139T=	GRCh38
NC_000002.11:g.128183715T= , CM000664.1:g.128183715T=	GRCh37
NC_000002.10:g.127900185T=	NCBI36
NG_016323.1:g.12720T= , LRG_599:g.12720T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.590T= MANE Select	ENSP00000234071.4:p.Leu197=
ENST00000234071.7:c.590T=	ENSP00000234071.3:p.Leu197=
ENST00000402125.2:c.121-2218T=
ENST00000409048.1:c.692T=	ENSP00000386679.1:p.Leu231=
ENST00000464089.1:n.176T=
NM_000312.3:c.590T= , LRG_599t1:c.590T=	NP_000303.1:p.Leu197=
XM_005263715.3:c.773T=	XP_005263772.1:p.Leu258=
XM_005263716.3:c.755T=	XP_005263773.1:p.Leu252=
XM_005263717.3:c.653T=	XP_005263774.1:p.Leu218=
XM_005263717.4:c.653T=	XP_005263774.1:p.Leu218=
XM_017004505.1:c.833T=	XP_016859994.1:p.Leu278=
XM_024453002.1:c.935T=	XP_024308770.1:p.Leu312=
XM_024453003.1:c.875T=	XP_024308771.1:p.Leu292=
XM_024453004.1:c.773T=	XP_024308772.1:p.Leu258=
XM_024453005.1:c.755T=	XP_024308773.1:p.Leu252=
XM_024453006.1:c.692T=	XP_024308774.1:p.Leu231=
XR_923313.2:n.4446A=
NM_000312.4:c.590T= MANE Select	NP_000303.1:p.Leu197=
NM_001375602.1:c.773T=	NP_001362531.1:p.Leu258=
NM_001375603.1:c.755T=	NP_001362532.1:p.Leu252=
NM_001375604.1:c.653T=	NP_001362533.1:p.Leu218=
NM_001375605.1:c.692T=	NP_001362534.1:p.Leu231=
NM_001375606.1:c.758T=	NP_001362535.1:p.Leu253=
NM_001375607.1:c.776T=	NP_001362536.1:p.Leu259=
NM_001375608.1:c.533T=	NP_001362537.1:p.Leu178=
NM_001375609.1:c.566T=	NP_001362538.1:p.Leu189=
NM_001375610.1:c.584T=	NP_001362539.1:p.Leu195=
NM_001375611.1:c.590T=	NP_001362540.1:p.Leu197=
NM_001375613.1:c.590T=	NP_001362542.1:p.Leu197=