Canonical Allele Identifier: CA348401171

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128183700A>T (hg19) ; chr2:g.127426124A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426124A>T , CM000664.2:g.127426124A>T	GRCh38
NC_000002.11:g.128183700A>T , CM000664.1:g.128183700A>T	GRCh37
NC_000002.10:g.127900170A>T	NCBI36
NG_016323.1:g.12705A>T , LRG_599:g.12705A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.575A>T MANE Select	ENSP00000234071.4:p.Lys192Met
ENST00000234071.7:c.575A>T	ENSP00000234071.3:p.Lys192Met
ENST00000402125.2:c.121-2233A>T
ENST00000409048.1:c.677A>T	ENSP00000386679.1:p.Lys226Met
ENST00000442644.5:c.518A>T	ENSP00000411241.1:p.Lys173Met
ENST00000464089.1:n.161A>T
NM_000312.3:c.575A>T , LRG_599t1:c.575A>T	NP_000303.1:p.Lys192Met
XM_005263715.3:c.758A>T	XP_005263772.1:p.Lys253Met
XM_005263716.3:c.740A>T	XP_005263773.1:p.Lys247Met
XM_005263717.3:c.638A>T	XP_005263774.1:p.Lys213Met
XM_005263717.4:c.638A>T	XP_005263774.1:p.Lys213Met
XM_017004505.1:c.818A>T	XP_016859994.1:p.Lys273Met
XM_024453002.1:c.920A>T	XP_024308770.1:p.Lys307Met
XM_024453003.1:c.860A>T	XP_024308771.1:p.Lys287Met
XM_024453004.1:c.758A>T	XP_024308772.1:p.Lys253Met
XM_024453005.1:c.740A>T	XP_024308773.1:p.Lys247Met
XM_024453006.1:c.677A>T	XP_024308774.1:p.Lys226Met
XR_923313.2:n.4461T>A
NM_000312.4:c.575A>T MANE Select	NP_000303.1:p.Lys192Met
NM_001375602.1:c.758A>T	NP_001362531.1:p.Lys253Met
NM_001375603.1:c.740A>T	NP_001362532.1:p.Lys247Met
NM_001375604.1:c.638A>T	NP_001362533.1:p.Lys213Met
NM_001375605.1:c.677A>T	NP_001362534.1:p.Lys226Met
NM_001375606.1:c.743A>T	NP_001362535.1:p.Lys248Met
NM_001375607.1:c.761A>T	NP_001362536.1:p.Lys254Met
NM_001375608.1:c.518A>T	NP_001362537.1:p.Lys173Met
NM_001375609.1:c.551A>T	NP_001362538.1:p.Lys184Met
NM_001375610.1:c.569A>T	NP_001362539.1:p.Lys190Met
NM_001375611.1:c.575A>T	NP_001362540.1:p.Lys192Met
NM_001375613.1:c.575A>T	NP_001362542.1:p.Lys192Met