Canonical Allele Identifier: CA1286883456

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426221_127426222delinsCT , CM000664.2:g.127426221_127426222delinsCT	GRCh38
NC_000002.11:g.128183797_128183798delinsCT , CM000664.1:g.128183797_128183798delinsCT	GRCh37
NC_000002.10:g.127900267_127900268delinsCT	NCBI36
NG_016323.1:g.12802_12803delinsCT , LRG_599:g.12802_12803delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.672_673delinsCT MANE Select	ENSP00000234071.4:p.Pro224=
ENST00000234071.7:c.672_673delinsCT	ENSP00000234071.3:p.Pro224=
ENST00000402125.2:c.121-2136_121-2135delinsCT
ENST00000409048.1:c.774_775delinsCT	ENSP00000386679.1:p.Pro258=
ENST00000464089.1:n.258_259delinsCT
NM_000312.3:c.672_673delinsCT , LRG_599t1:c.672_673delinsCT	NP_000303.1:p.Pro224=
XM_005263715.3:c.855_856delinsCT	XP_005263772.1:p.Pro285=
XM_005263716.3:c.837_838delinsCT	XP_005263773.1:p.Pro279=
XM_005263717.3:c.735_736delinsCT	XP_005263774.1:p.Pro245=
XM_005263717.4:c.735_736delinsCT	XP_005263774.1:p.Pro245=
XM_017004505.1:c.915_916delinsCT	XP_016859994.1:p.Pro305=
XM_024453002.1:c.1017_1018delinsCT	XP_024308770.1:p.Pro339=
XM_024453003.1:c.957_958delinsCT	XP_024308771.1:p.Pro319=
XM_024453004.1:c.855_856delinsCT	XP_024308772.1:p.Pro285=
XM_024453005.1:c.837_838delinsCT	XP_024308773.1:p.Pro279=
XM_024453006.1:c.774_775delinsCT	XP_024308774.1:p.Pro258=
XR_923313.2:n.4363_4364delinsAG
NM_000312.4:c.672_673delinsCT MANE Select	NP_000303.1:p.Pro224=
NM_001375602.1:c.855_856delinsCT	NP_001362531.1:p.Pro285=
NM_001375603.1:c.837_838delinsCT	NP_001362532.1:p.Pro279=
NM_001375604.1:c.735_736delinsCT	NP_001362533.1:p.Pro245=
NM_001375605.1:c.774_775delinsCT	NP_001362534.1:p.Pro258=
NM_001375606.1:c.840_841delinsCT	NP_001362535.1:p.Pro280=
NM_001375607.1:c.858_859delinsCT	NP_001362536.1:p.Pro286=
NM_001375608.1:c.615_616delinsCT	NP_001362537.1:p.Pro205=
NM_001375609.1:c.648_649delinsCT	NP_001362538.1:p.Pro216=
NM_001375610.1:c.666_667delinsCT	NP_001362539.1:p.Pro222=
NM_001375611.1:c.672_673delinsCT	NP_001362540.1:p.Pro224=
NM_001375613.1:c.672_673delinsCT	NP_001362542.1:p.Pro224=