Canonical Allele Identifier: CA428618198

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128183683C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426107C>G , CM000664.2:g.127426107C>G	GRCh38
NC_000002.11:g.128183683C>G , CM000664.1:g.128183683C>G	GRCh37
NC_000002.10:g.127900153C>G	NCBI36
NG_016323.1:g.12688C>G , LRG_599:g.12688C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.558C>G MANE Select	ENSP00000234071.4:p.Pro186=
ENST00000234071.7:c.558C>G	ENSP00000234071.3:p.Pro186=
ENST00000402125.2:c.121-2250C>G
ENST00000409048.1:c.660C>G	ENSP00000386679.1:p.Pro220=
ENST00000442644.5:c.501C>G	ENSP00000411241.1:p.Pro167=
ENST00000464089.1:n.144C>G
NM_000312.3:c.558C>G , LRG_599t1:c.558C>G	NP_000303.1:p.Pro186=
XM_005263715.3:c.741C>G	XP_005263772.1:p.Pro247=
XM_005263716.3:c.723C>G	XP_005263773.1:p.Pro241=
XM_005263717.3:c.621C>G	XP_005263774.1:p.Pro207=
XM_005263717.4:c.621C>G	XP_005263774.1:p.Pro207=
XM_017004505.1:c.801C>G	XP_016859994.1:p.Pro267=
XM_024453002.1:c.903C>G	XP_024308770.1:p.Pro301=
XM_024453003.1:c.843C>G	XP_024308771.1:p.Pro281=
XM_024453004.1:c.741C>G	XP_024308772.1:p.Pro247=
XM_024453005.1:c.723C>G	XP_024308773.1:p.Pro241=
XM_024453006.1:c.660C>G	XP_024308774.1:p.Pro220=
XR_923313.2:n.4478G>C
NM_000312.4:c.558C>G MANE Select	NP_000303.1:p.Pro186=
NM_001375602.1:c.741C>G	NP_001362531.1:p.Pro247=
NM_001375603.1:c.723C>G	NP_001362532.1:p.Pro241=
NM_001375604.1:c.621C>G	NP_001362533.1:p.Pro207=
NM_001375605.1:c.660C>G	NP_001362534.1:p.Pro220=
NM_001375606.1:c.726C>G	NP_001362535.1:p.Pro242=
NM_001375607.1:c.744C>G	NP_001362536.1:p.Pro248=
NM_001375608.1:c.501C>G	NP_001362537.1:p.Pro167=
NM_001375609.1:c.534C>G	NP_001362538.1:p.Pro178=
NM_001375610.1:c.552C>G	NP_001362539.1:p.Pro184=
NM_001375611.1:c.558C>G	NP_001362540.1:p.Pro186=
NM_001375613.1:c.558C>G	NP_001362542.1:p.Pro186=