Canonical Allele Identifier: CA348401417

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128183740A>T (hg19) ; chr2:g.127426164A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426164A>T , CM000664.2:g.127426164A>T	GRCh38
NC_000002.11:g.128183740A>T , CM000664.1:g.128183740A>T	GRCh37
NC_000002.10:g.127900210A>T	NCBI36
NG_016323.1:g.12745A>T , LRG_599:g.12745A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.615A>T MANE Select	ENSP00000234071.4:p.Glu205Asp
ENST00000234071.7:c.615A>T	ENSP00000234071.3:p.Glu205Asp
ENST00000402125.2:c.121-2193A>T
ENST00000409048.1:c.717A>T	ENSP00000386679.1:p.Glu239Asp
ENST00000464089.1:n.201A>T
NM_000312.3:c.615A>T , LRG_599t1:c.615A>T	NP_000303.1:p.Glu205Asp
XM_005263715.3:c.798A>T	XP_005263772.1:p.Glu266Asp
XM_005263716.3:c.780A>T	XP_005263773.1:p.Glu260Asp
XM_005263717.3:c.678A>T	XP_005263774.1:p.Glu226Asp
XM_005263717.4:c.678A>T	XP_005263774.1:p.Glu226Asp
XM_017004505.1:c.858A>T	XP_016859994.1:p.Glu286Asp
XM_024453002.1:c.960A>T	XP_024308770.1:p.Glu320Asp
XM_024453003.1:c.900A>T	XP_024308771.1:p.Glu300Asp
XM_024453004.1:c.798A>T	XP_024308772.1:p.Glu266Asp
XM_024453005.1:c.780A>T	XP_024308773.1:p.Glu260Asp
XM_024453006.1:c.717A>T	XP_024308774.1:p.Glu239Asp
XR_923313.2:n.4421T>A
NM_000312.4:c.615A>T MANE Select	NP_000303.1:p.Glu205Asp
NM_001375602.1:c.798A>T	NP_001362531.1:p.Glu266Asp
NM_001375603.1:c.780A>T	NP_001362532.1:p.Glu260Asp
NM_001375604.1:c.678A>T	NP_001362533.1:p.Glu226Asp
NM_001375605.1:c.717A>T	NP_001362534.1:p.Glu239Asp
NM_001375606.1:c.783A>T	NP_001362535.1:p.Glu261Asp
NM_001375607.1:c.801A>T	NP_001362536.1:p.Glu267Asp
NM_001375608.1:c.558A>T	NP_001362537.1:p.Glu186Asp
NM_001375609.1:c.591A>T	NP_001362538.1:p.Glu197Asp
NM_001375610.1:c.609A>T	NP_001362539.1:p.Glu203Asp
NM_001375611.1:c.615A>T	NP_001362540.1:p.Glu205Asp
NM_001375613.1:c.615A>T	NP_001362542.1:p.Glu205Asp