Canonical Allele Identifier: CA1975539288

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614500G= , CM000673.2:g.57614500G=	GRCh38
NC_000011.9:g.57381973G= , CM000673.1:g.57381973G=	GRCh37
NC_000011.8:g.57138549G=	NCBI36
NG_009625.1:g.21947G= , LRG_105:g.21947G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1422G= MANE Select	ENSP00000278407.4:p.Gln474=
ENST00000528996.2:c.*319G=	ENSP00000431226.2:n.*319G=
ENST00000531605.2:c.*1198G=	ENSP00000503752.1:n.*1198G=
ENST00000619430.2:c.1218G=	ENSP00000478572.2:p.Gln406=
ENST00000676670.1:c.1422G=	ENSP00000504807.1:p.Gln474=
ENST00000676741.1:n.2504G=
ENST00000677624.1:c.*842G=	ENSP00000503979.1:n.*842G=
ENST00000677625.1:c.1368G=	ENSP00000502857.1:p.Gln456=
ENST00000677856.1:n.1675G=
ENST00000677915.1:c.*319G=	ENSP00000503118.1:n.*319G=
ENST00000678533.1:c.*976G=	ENSP00000503873.1:n.*976G=
ENST00000678592.1:c.*362G=	ENSP00000504424.1:n.*362G=
ENST00000278407.8:c.1422G=	ENSP00000278407.4:p.Gln474=
ENST00000340687.10:c.1311G=	ENSP00000341861.6:p.Gln437=
ENST00000378323.8:c.1437G=	ENSP00000367574.4:p.Gln479=
ENST00000378324.6:c.1266G=	ENSP00000367575.2:p.Gln422=
ENST00000403558.1:c.1551G=	ENSP00000384420.1:p.Gln517=
ENST00000528996.1:c.623G=	ENSP00000431226.1:n.623G=
ENST00000530113.1:n.879G=
ENST00000531133.5:c.923G=	ENSP00000435431.1:n.923G=
ENST00000531797.5:c.*447G=	ENSP00000432554.1:n.*447G=
ENST00000619430.1:c.553G=	ENSP00000478572.1:n.553G=
NM_000062.2:c.1422G= , LRG_105t1:c.1422G=	NP_000053.2:p.Gln474=
NM_001032295.1:c.1422G=	NP_001027466.1:p.Gln474=
NM_000062.3:c.1422G= MANE Select	NP_000053.2:p.Gln474=
NM_001032295.2:c.1422G=	NP_001027466.1:p.Gln474=