Canonical Allele Identifier: CA428618556

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128184722A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127427146A>T , CM000664.2:g.127427146A>T	GRCh38
NC_000002.11:g.128184722A>T , CM000664.1:g.128184722A>T	GRCh37
NC_000002.10:g.127901192A>T	NCBI36
NG_016323.1:g.13727A>T , LRG_599:g.13727A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.720A>T MANE Select	ENSP00000234071.4:p.Ala240=
ENST00000234071.7:c.720A>T	ENSP00000234071.3:p.Ala240=
ENST00000402125.2:c.121-1211A>T
ENST00000409048.1:c.822A>T	ENSP00000386679.1:p.Ala274=
NM_000312.3:c.720A>T , LRG_599t1:c.720A>T	NP_000303.1:p.Ala240=
XM_005263715.3:c.903A>T	XP_005263772.1:p.Ala301=
XM_005263716.3:c.885A>T	XP_005263773.1:p.Ala295=
XM_005263717.3:c.783A>T	XP_005263774.1:p.Ala261=
XR_923313.1:n.1486-758T>A
XM_005263717.4:c.783A>T	XP_005263774.1:p.Ala261=
XM_017004505.1:c.963A>T	XP_016859994.1:p.Ala321=
XM_024453002.1:c.1065A>T	XP_024308770.1:p.Ala355=
XM_024453003.1:c.1005A>T	XP_024308771.1:p.Ala335=
XM_024453004.1:c.903A>T	XP_024308772.1:p.Ala301=
XM_024453005.1:c.885A>T	XP_024308773.1:p.Ala295=
XM_024453006.1:c.822A>T	XP_024308774.1:p.Ala274=
XR_923313.2:n.4197-758T>A
NM_000312.4:c.720A>T MANE Select	NP_000303.1:p.Ala240=
NM_001375602.1:c.903A>T	NP_001362531.1:p.Ala301=
NM_001375603.1:c.885A>T	NP_001362532.1:p.Ala295=
NM_001375604.1:c.783A>T	NP_001362533.1:p.Ala261=
NM_001375605.1:c.822A>T	NP_001362534.1:p.Ala274=
NM_001375606.1:c.888A>T	NP_001362535.1:p.Ala296=
NM_001375607.1:c.906A>T	NP_001362536.1:p.Ala302=
NM_001375608.1:c.663A>T	NP_001362537.1:p.Ala221=
NM_001375609.1:c.696A>T	NP_001362538.1:p.Ala232=
NM_001375610.1:c.714A>T	NP_001362539.1:p.Ala238=
NM_001375611.1:c.720A>T	NP_001362540.1:p.Ala240=
NM_001375613.1:c.720A>T	NP_001362542.1:p.Ala240=