Canonical Allele Identifier: CA428618918

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186048C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428472C>T , CM000664.2:g.127428472C>T	GRCh38
NC_000002.11:g.128186048C>T , CM000664.1:g.128186048C>T	GRCh37
NC_000002.10:g.127902518C>T	NCBI36
NG_016323.1:g.15053C>T , LRG_599:g.15053C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.912C>T MANE Select	ENSP00000234071.4:p.His304=
ENST00000234071.7:c.912C>T	ENSP00000234071.3:p.His304=
ENST00000402125.2:c.236C>T
ENST00000409048.1:c.1014C>T	ENSP00000386679.1:p.His338=
NM_000312.3:c.912C>T , LRG_599t1:c.912C>T	NP_000303.1:p.His304=
XM_005263715.3:c.1095C>T	XP_005263772.1:p.His365=
XM_005263716.3:c.1077C>T	XP_005263773.1:p.His359=
XM_005263717.3:c.975C>T	XP_005263774.1:p.His325=
XR_923313.1:n.1332-208G>A
XM_005263717.4:c.975C>T	XP_005263774.1:p.His325=
XM_017004505.1:c.1155C>T	XP_016859994.1:p.His385=
XM_024453002.1:c.1257C>T	XP_024308770.1:p.His419=
XM_024453003.1:c.1197C>T	XP_024308771.1:p.His399=
XM_024453004.1:c.1095C>T	XP_024308772.1:p.His365=
XM_024453005.1:c.1077C>T	XP_024308773.1:p.His359=
XM_024453006.1:c.1014C>T	XP_024308774.1:p.His338=
XR_001739705.1:n.3607-208G>A
XR_923313.2:n.4043-208G>A
NM_000312.4:c.912C>T MANE Select	NP_000303.1:p.His304=
NM_001375602.1:c.1095C>T	NP_001362531.1:p.His365=
NM_001375603.1:c.1077C>T	NP_001362532.1:p.His359=
NM_001375604.1:c.975C>T	NP_001362533.1:p.His325=
NM_001375605.1:c.1014C>T	NP_001362534.1:p.His338=
NM_001375606.1:c.1080C>T	NP_001362535.1:p.His360=
NM_001375607.1:c.1098C>T	NP_001362536.1:p.His366=
NM_001375608.1:c.855C>T	NP_001362537.1:p.His285=
NM_001375609.1:c.888C>T	NP_001362538.1:p.His296=
NM_001375610.1:c.906C>T	NP_001362539.1:p.His302=
NM_001375611.1:c.912C>T	NP_001362540.1:p.His304=
NM_001375613.1:c.912C>T	NP_001362542.1:p.His304=