Canonical Allele Identifier: CA1286881241

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127421880_127421890delinsGGGAGAAAATC , CM000664.2:g.127421880_127421890delinsGGGAGAAAATC	GRCh38
NC_000002.11:g.128179456_128179466delinsGGGAGAAAATC , CM000664.1:g.128179456_128179466delinsGGGAGAAAATC	GRCh37
NC_000002.10:g.127895926_127895936delinsGGGAGAAAATC	NCBI36
NG_016323.1:g.8461_8471delinsGGGAGAAAATC , LRG_599:g.8461_8471delinsGGGAGAAAATC

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.237+431_237+441delinsGGGAGAAAATC MANE Select	ENSP00000234071.4:n.237+431_237+441delins...
ENST00000234071.7:c.237+431_237+441delinsGGGAGAAAATC	ENSP00000234071.3:n.237+431_237+441delins...
ENST00000409048.1:c.237+431_237+441delinsGGGAGAAAATC	ENSP00000386679.1:n.237+431_237+441delins...
ENST00000419985.5:c.*43+431_*43+441delinsGGGAGAAAATC	ENSP00000392606.1:n.*43+431_*43+441delins...
ENST00000427769.5:c.237+431_237+441delinsGGGAGAAAATC	ENSP00000406295.1:n.237+431_237+441delins...
ENST00000429925.5:c.237+431_237+441delinsGGGAGAAAATC	ENSP00000412697.1:n.237+431_237+441delins...
ENST00000431364.1:c.*43+431_*43+441delinsGGGAGAAAATC	ENSP00000391220.1:n.*43+431_*43+441delins...
ENST00000442644.5:c.237+431_237+441delinsGGGAGAAAATC	ENSP00000411241.1:n.237+431_237+441delins...
ENST00000474030.5:n.320+431_320+441delinsGGGAGAAAATC
NM_000312.3:c.237+431_237+441delinsGGGAGAAAATC , LRG_599t1:c.237+431_237+441delinsGGGAGAAAATC	NP_000303.1:n.237+431_237+441delinsGGGAGA...
XM_005263715.3:c.420+431_420+441delinsGGGAGAAAATC	XP_005263772.1:n.420+431_420+441delinsGGG...
XM_005263716.3:c.300+431_300+441delinsGGGAGAAAATC	XP_005263773.1:n.300+431_300+441delinsGGG...
XM_005263717.3:c.300+431_300+441delinsGGGAGAAAATC	XP_005263774.1:n.300+431_300+441delinsGGG...
XM_005263717.4:c.300+431_300+441delinsGGGAGAAAATC	XP_005263774.1:n.300+431_300+441delinsGGG...
XM_017004505.1:c.480+431_480+441delinsGGGAGAAAATC	XP_016859994.1:n.480+431_480+441delinsGGG...
XM_024453002.1:c.480+431_480+441delinsGGGAGAAAATC	XP_024308770.1:n.480+431_480+441delinsGGG...
XM_024453003.1:c.420+431_420+441delinsGGGAGAAAATC	XP_024308771.1:n.420+431_420+441delinsGGG...
XM_024453004.1:c.420+431_420+441delinsGGGAGAAAATC	XP_024308772.1:n.420+431_420+441delinsGGG...
XM_024453005.1:c.300+431_300+441delinsGGGAGAAAATC	XP_024308773.1:n.300+431_300+441delinsGGG...
XM_024453006.1:c.237+431_237+441delinsGGGAGAAAATC	XP_024308774.1:n.237+431_237+441delinsGGG...
NM_000312.4:c.237+431_237+441delinsGGGAGAAAATC MANE Select	NP_000303.1:n.237+431_237+441delinsGGGAGA...
NM_001375602.1:c.420+431_420+441delinsGGGAGAAAATC	NP_001362531.1:n.420+431_420+441delinsGGG...
NM_001375603.1:c.300+431_300+441delinsGGGAGAAAATC	NP_001362532.1:n.300+431_300+441delinsGGG...
NM_001375604.1:c.300+431_300+441delinsGGGAGAAAATC	NP_001362533.1:n.300+431_300+441delinsGGG...
NM_001375605.1:c.237+431_237+441delinsGGGAGAAAATC	NP_001362534.1:n.237+431_237+441delinsGGG...
NM_001375606.1:c.300+431_300+441delinsGGGAGAAAATC	NP_001362535.1:n.300+431_300+441delinsGGG...
NM_001375607.1:c.321+431_321+441delinsGGGAGAAAATC	NP_001362536.1:n.321+431_321+441delinsGGG...
NM_001375608.1:c.237+431_237+441delinsGGGAGAAAATC	NP_001362537.1:n.237+431_237+441delinsGGG...
NM_001375609.1:c.213+431_213+441delinsGGGAGAAAATC	NP_001362538.1:n.213+431_213+441delinsGGG...
NM_001375610.1:c.231+431_231+441delinsGGGAGAAAATC	NP_001362539.1:n.231+431_231+441delinsGGG...
NM_001375611.1:c.237+431_237+441delinsGGGAGAAAATC	NP_001362540.1:n.237+431_237+441delinsGGG...
NM_001375613.1:c.237+431_237+441delinsGGGAGAAAATC	NP_001362542.1:n.237+431_237+441delinsGGG...