Canonical Allele Identifier: CA428618915

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186045G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428469G>A , CM000664.2:g.127428469G>A	GRCh38
NC_000002.11:g.128186045G>A , CM000664.1:g.128186045G>A	GRCh37
NC_000002.10:g.127902515G>A	NCBI36
NG_016323.1:g.15050G>A , LRG_599:g.15050G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.909G>A MANE Select	ENSP00000234071.4:p.Leu303=
ENST00000234071.7:c.909G>A	ENSP00000234071.3:p.Leu303=
ENST00000402125.2:c.233G>A
ENST00000409048.1:c.1011G>A	ENSP00000386679.1:p.Leu337=
NM_000312.3:c.909G>A , LRG_599t1:c.909G>A	NP_000303.1:p.Leu303=
XM_005263715.3:c.1092G>A	XP_005263772.1:p.Leu364=
XM_005263716.3:c.1074G>A	XP_005263773.1:p.Leu358=
XM_005263717.3:c.972G>A	XP_005263774.1:p.Leu324=
XR_923313.1:n.1332-205C>T
XM_005263717.4:c.972G>A	XP_005263774.1:p.Leu324=
XM_017004505.1:c.1152G>A	XP_016859994.1:p.Leu384=
XM_024453002.1:c.1254G>A	XP_024308770.1:p.Leu418=
XM_024453003.1:c.1194G>A	XP_024308771.1:p.Leu398=
XM_024453004.1:c.1092G>A	XP_024308772.1:p.Leu364=
XM_024453005.1:c.1074G>A	XP_024308773.1:p.Leu358=
XM_024453006.1:c.1011G>A	XP_024308774.1:p.Leu337=
XR_001739705.1:n.3607-205C>T
XR_923313.2:n.4043-205C>T
NM_000312.4:c.909G>A MANE Select	NP_000303.1:p.Leu303=
NM_001375602.1:c.1092G>A	NP_001362531.1:p.Leu364=
NM_001375603.1:c.1074G>A	NP_001362532.1:p.Leu358=
NM_001375604.1:c.972G>A	NP_001362533.1:p.Leu324=
NM_001375605.1:c.1011G>A	NP_001362534.1:p.Leu337=
NM_001375606.1:c.1077G>A	NP_001362535.1:p.Leu359=
NM_001375607.1:c.1095G>A	NP_001362536.1:p.Leu365=
NM_001375608.1:c.852G>A	NP_001362537.1:p.Leu284=
NM_001375609.1:c.885G>A	NP_001362538.1:p.Leu295=
NM_001375610.1:c.903G>A	NP_001362539.1:p.Leu301=
NM_001375611.1:c.909G>A	NP_001362540.1:p.Leu303=
NM_001375613.1:c.909G>A	NP_001362542.1:p.Leu303=