Canonical Allele Identifier: CA428618882

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128185976G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428400G>C , CM000664.2:g.127428400G>C	GRCh38
NC_000002.11:g.128185976G>C , CM000664.1:g.128185976G>C	GRCh37
NC_000002.10:g.127902446G>C	NCBI36
NG_016323.1:g.14981G>C , LRG_599:g.14981G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.840G>C MANE Select	ENSP00000234071.4:p.Leu280=
ENST00000234071.7:c.840G>C	ENSP00000234071.3:p.Leu280=
ENST00000402125.2:c.164G>C
ENST00000409048.1:c.942G>C	ENSP00000386679.1:p.Leu314=
NM_000312.3:c.840G>C , LRG_599t1:c.840G>C	NP_000303.1:p.Leu280=
XM_005263715.3:c.1023G>C	XP_005263772.1:p.Leu341=
XM_005263716.3:c.1005G>C	XP_005263773.1:p.Leu335=
XM_005263717.3:c.903G>C	XP_005263774.1:p.Leu301=
XR_923313.1:n.1332-136C>G
XM_005263717.4:c.903G>C	XP_005263774.1:p.Leu301=
XM_017004505.1:c.1083G>C	XP_016859994.1:p.Leu361=
XM_024453002.1:c.1185G>C	XP_024308770.1:p.Leu395=
XM_024453003.1:c.1125G>C	XP_024308771.1:p.Leu375=
XM_024453004.1:c.1023G>C	XP_024308772.1:p.Leu341=
XM_024453005.1:c.1005G>C	XP_024308773.1:p.Leu335=
XM_024453006.1:c.942G>C	XP_024308774.1:p.Leu314=
XR_001739705.1:n.3607-136C>G
XR_923313.2:n.4043-136C>G
NM_000312.4:c.840G>C MANE Select	NP_000303.1:p.Leu280=
NM_001375602.1:c.1023G>C	NP_001362531.1:p.Leu341=
NM_001375603.1:c.1005G>C	NP_001362532.1:p.Leu335=
NM_001375604.1:c.903G>C	NP_001362533.1:p.Leu301=
NM_001375605.1:c.942G>C	NP_001362534.1:p.Leu314=
NM_001375606.1:c.1008G>C	NP_001362535.1:p.Leu336=
NM_001375607.1:c.1026G>C	NP_001362536.1:p.Leu342=
NM_001375608.1:c.783G>C	NP_001362537.1:p.Leu261=
NM_001375609.1:c.816G>C	NP_001362538.1:p.Leu272=
NM_001375610.1:c.834G>C	NP_001362539.1:p.Leu278=
NM_001375611.1:c.840G>C	NP_001362540.1:p.Leu280=
NM_001375613.1:c.840G>C	NP_001362542.1:p.Leu280=