Canonical Allele Identifier: CA1286883453

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426214A= , CM000664.2:g.127426214A=	GRCh38
NC_000002.11:g.128183790A= , CM000664.1:g.128183790A=	GRCh37
NC_000002.10:g.127900260A=	NCBI36
NG_016323.1:g.12795A= , LRG_599:g.12795A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.665A= MANE Select	ENSP00000234071.4:p.Asp222=
ENST00000234071.7:c.665A=	ENSP00000234071.3:p.Asp222=
ENST00000402125.2:c.121-2143A=
ENST00000409048.1:c.767A=	ENSP00000386679.1:p.Asp256=
ENST00000464089.1:n.251A=
NM_000312.3:c.665A= , LRG_599t1:c.665A=	NP_000303.1:p.Asp222=
XM_005263715.3:c.848A=	XP_005263772.1:p.Asp283=
XM_005263716.3:c.830A=	XP_005263773.1:p.Asp277=
XM_005263717.3:c.728A=	XP_005263774.1:p.Asp243=
XM_005263717.4:c.728A=	XP_005263774.1:p.Asp243=
XM_017004505.1:c.908A=	XP_016859994.1:p.Asp303=
XM_024453002.1:c.1010A=	XP_024308770.1:p.Asp337=
XM_024453003.1:c.950A=	XP_024308771.1:p.Asp317=
XM_024453004.1:c.848A=	XP_024308772.1:p.Asp283=
XM_024453005.1:c.830A=	XP_024308773.1:p.Asp277=
XM_024453006.1:c.767A=	XP_024308774.1:p.Asp256=
XR_923313.2:n.4371T=
NM_000312.4:c.665A= MANE Select	NP_000303.1:p.Asp222=
NM_001375602.1:c.848A=	NP_001362531.1:p.Asp283=
NM_001375603.1:c.830A=	NP_001362532.1:p.Asp277=
NM_001375604.1:c.728A=	NP_001362533.1:p.Asp243=
NM_001375605.1:c.767A=	NP_001362534.1:p.Asp256=
NM_001375606.1:c.833A=	NP_001362535.1:p.Asp278=
NM_001375607.1:c.851A=	NP_001362536.1:p.Asp284=
NM_001375608.1:c.608A=	NP_001362537.1:p.Asp203=
NM_001375609.1:c.641A=	NP_001362538.1:p.Asp214=
NM_001375610.1:c.659A=	NP_001362539.1:p.Asp220=
NM_001375611.1:c.665A=	NP_001362540.1:p.Asp222=
NM_001375613.1:c.665A=	NP_001362542.1:p.Asp222=