Canonical Allele Identifier: CA428618189

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128183677G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426101G>T , CM000664.2:g.127426101G>T	GRCh38
NC_000002.11:g.128183677G>T , CM000664.1:g.128183677G>T	GRCh37
NC_000002.10:g.127900147G>T	NCBI36
NG_016323.1:g.12682G>T , LRG_599:g.12682G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.552G>T MANE Select	ENSP00000234071.4:p.Gly184=
ENST00000234071.7:c.552G>T	ENSP00000234071.3:p.Gly184=
ENST00000402125.2:c.121-2256G>T
ENST00000409048.1:c.654G>T	ENSP00000386679.1:p.Gly218=
ENST00000442644.5:c.495G>T	ENSP00000411241.1:p.Gly165=
ENST00000464089.1:n.138G>T
NM_000312.3:c.552G>T , LRG_599t1:c.552G>T	NP_000303.1:p.Gly184=
XM_005263715.3:c.735G>T	XP_005263772.1:p.Gly245=
XM_005263716.3:c.717G>T	XP_005263773.1:p.Gly239=
XM_005263717.3:c.615G>T	XP_005263774.1:p.Gly205=
XM_005263717.4:c.615G>T	XP_005263774.1:p.Gly205=
XM_017004505.1:c.795G>T	XP_016859994.1:p.Gly265=
XM_024453002.1:c.897G>T	XP_024308770.1:p.Gly299=
XM_024453003.1:c.837G>T	XP_024308771.1:p.Gly279=
XM_024453004.1:c.735G>T	XP_024308772.1:p.Gly245=
XM_024453005.1:c.717G>T	XP_024308773.1:p.Gly239=
XM_024453006.1:c.654G>T	XP_024308774.1:p.Gly218=
XR_923313.2:n.4484C>A
NM_000312.4:c.552G>T MANE Select	NP_000303.1:p.Gly184=
NM_001375602.1:c.735G>T	NP_001362531.1:p.Gly245=
NM_001375603.1:c.717G>T	NP_001362532.1:p.Gly239=
NM_001375604.1:c.615G>T	NP_001362533.1:p.Gly205=
NM_001375605.1:c.654G>T	NP_001362534.1:p.Gly218=
NM_001375606.1:c.720G>T	NP_001362535.1:p.Gly240=
NM_001375607.1:c.738G>T	NP_001362536.1:p.Gly246=
NM_001375608.1:c.495G>T	NP_001362537.1:p.Gly165=
NM_001375609.1:c.528G>T	NP_001362538.1:p.Gly176=
NM_001375610.1:c.546G>T	NP_001362539.1:p.Gly182=
NM_001375611.1:c.552G>T	NP_001362540.1:p.Gly184=
NM_001375613.1:c.552G>T	NP_001362542.1:p.Gly184=