Canonical Allele Identifier: CA348405472

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186154A>T (hg19) ; chr2:g.127428578A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428578A>T , CM000664.2:g.127428578A>T	GRCh38
NC_000002.11:g.128186154A>T , CM000664.1:g.128186154A>T	GRCh37
NC_000002.10:g.127902624A>T	NCBI36
NG_016323.1:g.15159A>T , LRG_599:g.15159A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1018A>T MANE Select	ENSP00000234071.4:p.Thr340Ser
ENST00000234071.7:c.1018A>T	ENSP00000234071.3:p.Thr340Ser
ENST00000402125.2:c.342A>T
ENST00000409048.1:c.1120A>T	ENSP00000386679.1:p.Thr374Ser
NM_000312.3:c.1018A>T , LRG_599t1:c.1018A>T	NP_000303.1:p.Thr340Ser
XM_005263715.3:c.1201A>T	XP_005263772.1:p.Thr401Ser
XM_005263716.3:c.1183A>T	XP_005263773.1:p.Thr395Ser
XM_005263717.3:c.1081A>T	XP_005263774.1:p.Thr361Ser
XR_923313.1:n.1332-314T>A
XM_005263717.4:c.1081A>T	XP_005263774.1:p.Thr361Ser
XM_017004505.1:c.1261A>T	XP_016859994.1:p.Thr421Ser
XM_024453002.1:c.1363A>T	XP_024308770.1:p.Thr455Ser
XM_024453003.1:c.1303A>T	XP_024308771.1:p.Thr435Ser
XM_024453004.1:c.1201A>T	XP_024308772.1:p.Thr401Ser
XM_024453005.1:c.1183A>T	XP_024308773.1:p.Thr395Ser
XM_024453006.1:c.1120A>T	XP_024308774.1:p.Thr374Ser
XR_001739705.1:n.3607-314T>A
XR_923313.2:n.4043-314T>A
NM_000312.4:c.1018A>T MANE Select	NP_000303.1:p.Thr340Ser
NM_001375602.1:c.1201A>T	NP_001362531.1:p.Thr401Ser
NM_001375603.1:c.1183A>T	NP_001362532.1:p.Thr395Ser
NM_001375604.1:c.1081A>T	NP_001362533.1:p.Thr361Ser
NM_001375605.1:c.1120A>T	NP_001362534.1:p.Thr374Ser
NM_001375606.1:c.1186A>T	NP_001362535.1:p.Thr396Ser
NM_001375607.1:c.1204A>T	NP_001362536.1:p.Thr402Ser
NM_001375608.1:c.961A>T	NP_001362537.1:p.Thr321Ser
NM_001375609.1:c.994A>T	NP_001362538.1:p.Thr332Ser
NM_001375610.1:c.1012A>T	NP_001362539.1:p.Thr338Ser
NM_001375611.1:c.1018A>T	NP_001362540.1:p.Thr340Ser
NM_001375613.1:c.1018A>T	NP_001362542.1:p.Thr340Ser