Canonical Allele Identifier: CA756625384

Gene: PROC

Linked Data

• dbSNP Id: rs1467821415
• MyVariant Identifiers: chr2:g.128178566_128178567insTA (hg19) ; chr2:g.127420990_127420991insTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127420991_127420992dup , CM000664.2:g.127420991_127420992dup	GRCh38
NC_000002.11:g.128178567_128178568dup , CM000664.1:g.128178567_128178568dup	GRCh37
NC_000002.10:g.127895037_127895038dup	NCBI36
NG_016323.1:g.7572_7573dup , LRG_599:g.7572_7573dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.71-292_71-291dup MANE Select	ENSP00000234071.4:n.71-292_71-291dup
ENST00000234071.7:c.71-292_71-291dup	ENSP00000234071.3:n.71-292_71-291dup
ENST00000409048.1:c.71-292_71-291dup	ENSP00000386679.1:n.71-292_71-291dup
ENST00000419985.5:c.71-327_71-326dup	ENSP00000392606.1:n.71-327_71-326dup
ENST00000427769.5:c.71-292_71-291dup	ENSP00000406295.1:n.71-292_71-291dup
ENST00000429925.5:c.71-292_71-291dup	ENSP00000412697.1:n.71-292_71-291dup
ENST00000431364.1:c.71-327_71-326dup	ENSP00000391220.1:n.71-327_71-326dup
ENST00000442644.5:c.71-292_71-291dup	ENSP00000411241.1:n.71-292_71-291dup
ENST00000474030.5:n.154-292_154-291dup
NM_000312.3:c.71-292_71-291dup , LRG_599t1:c.71-292_71-291dup	NP_000303.1:n.71-292_71-291dup
XM_005263715.3:c.254-292_254-291dup	XP_005263772.1:n.254-292_254-291dup
XM_005263716.3:c.134-292_134-291dup	XP_005263773.1:n.134-292_134-291dup
XM_005263717.3:c.134-292_134-291dup	XP_005263774.1:n.134-292_134-291dup
XM_005263717.4:c.134-292_134-291dup	XP_005263774.1:n.134-292_134-291dup
XM_017004505.1:c.349-327_349-326dup	XP_016859994.1:n.349-327_349-326dup
XM_024453002.1:c.349-327_349-326dup	XP_024308770.1:n.349-327_349-326dup
XM_024453003.1:c.254-292_254-291dup	XP_024308771.1:n.254-292_254-291dup
XM_024453004.1:c.254-292_254-291dup	XP_024308772.1:n.254-292_254-291dup
XM_024453005.1:c.134-292_134-291dup	XP_024308773.1:n.134-292_134-291dup
XM_024453006.1:c.71-292_71-291dup	XP_024308774.1:n.71-292_71-291dup
NM_000312.4:c.71-292_71-291dup MANE Select	NP_000303.1:n.71-292_71-291dup
NM_001375602.1:c.254-292_254-291dup	NP_001362531.1:n.254-292_254-291dup
NM_001375603.1:c.134-292_134-291dup	NP_001362532.1:n.134-292_134-291dup
NM_001375604.1:c.134-292_134-291dup	NP_001362533.1:n.134-292_134-291dup
NM_001375605.1:c.71-292_71-291dup	NP_001362534.1:n.71-292_71-291dup
NM_001375606.1:c.134-292_134-291dup	NP_001362535.1:n.134-292_134-291dup
NM_001375607.1:c.190-327_190-326dup	NP_001362536.1:n.190-327_190-326dup
NM_001375608.1:c.71-292_71-291dup	NP_001362537.1:n.71-292_71-291dup
NM_001375609.1:c.47-292_47-291dup	NP_001362538.1:n.47-292_47-291dup
NM_001375610.1:c.71-298_71-297dup	NP_001362539.1:n.71-298_71-297dup
NM_001375611.1:c.71-292_71-291dup	NP_001362540.1:n.71-292_71-291dup
NM_001375613.1:c.71-292_71-291dup	NP_001362542.1:n.71-292_71-291dup