Canonical Allele Identifier: CA348401373

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128183733A>G (hg19) ; chr2:g.127426157A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426157A>G , CM000664.2:g.127426157A>G	GRCh38
NC_000002.11:g.128183733A>G , CM000664.1:g.128183733A>G	GRCh37
NC_000002.10:g.127900203A>G	NCBI36
NG_016323.1:g.12738A>G , LRG_599:g.12738A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.608A>G MANE Select	ENSP00000234071.4:p.Asp203Gly
ENST00000234071.7:c.608A>G	ENSP00000234071.3:p.Asp203Gly
ENST00000402125.2:c.121-2200A>G
ENST00000409048.1:c.710A>G	ENSP00000386679.1:p.Asp237Gly
ENST00000464089.1:n.194A>G
NM_000312.3:c.608A>G , LRG_599t1:c.608A>G	NP_000303.1:p.Asp203Gly
XM_005263715.3:c.791A>G	XP_005263772.1:p.Asp264Gly
XM_005263716.3:c.773A>G	XP_005263773.1:p.Asp258Gly
XM_005263717.3:c.671A>G	XP_005263774.1:p.Asp224Gly
XM_005263717.4:c.671A>G	XP_005263774.1:p.Asp224Gly
XM_017004505.1:c.851A>G	XP_016859994.1:p.Asp284Gly
XM_024453002.1:c.953A>G	XP_024308770.1:p.Asp318Gly
XM_024453003.1:c.893A>G	XP_024308771.1:p.Asp298Gly
XM_024453004.1:c.791A>G	XP_024308772.1:p.Asp264Gly
XM_024453005.1:c.773A>G	XP_024308773.1:p.Asp258Gly
XM_024453006.1:c.710A>G	XP_024308774.1:p.Asp237Gly
XR_923313.2:n.4428T>C
NM_000312.4:c.608A>G MANE Select	NP_000303.1:p.Asp203Gly
NM_001375602.1:c.791A>G	NP_001362531.1:p.Asp264Gly
NM_001375603.1:c.773A>G	NP_001362532.1:p.Asp258Gly
NM_001375604.1:c.671A>G	NP_001362533.1:p.Asp224Gly
NM_001375605.1:c.710A>G	NP_001362534.1:p.Asp237Gly
NM_001375606.1:c.776A>G	NP_001362535.1:p.Asp259Gly
NM_001375607.1:c.794A>G	NP_001362536.1:p.Asp265Gly
NM_001375608.1:c.551A>G	NP_001362537.1:p.Asp184Gly
NM_001375609.1:c.584A>G	NP_001362538.1:p.Asp195Gly
NM_001375610.1:c.602A>G	NP_001362539.1:p.Asp201Gly
NM_001375611.1:c.608A>G	NP_001362540.1:p.Asp203Gly
NM_001375613.1:c.608A>G	NP_001362542.1:p.Asp203Gly