Canonical Allele Identifier: CA380690252

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381822A>C (hg19) ; chr11:g.57614349A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614349A>C , CM000673.2:g.57614349A>C	GRCh38
NC_000011.9:g.57381822A>C , CM000673.1:g.57381822A>C	GRCh37
NC_000011.8:g.57138398A>C	NCBI36
NG_009625.1:g.21796A>C , LRG_105:g.21796A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1271A>C MANE Select	ENSP00000278407.4:p.Asp424Ala
ENST00000528996.2:c.*168A>C	ENSP00000431226.2:n.*168A>C
ENST00000531605.2:c.*1047A>C	ENSP00000503752.1:n.*1047A>C
ENST00000619430.2:c.1067A>C	ENSP00000478572.2:p.Asp356Ala
ENST00000676670.1:c.1271A>C	ENSP00000504807.1:p.Asp424Ala
ENST00000676741.1:n.2353A>C
ENST00000677624.1:c.*691A>C	ENSP00000503979.1:n.*691A>C
ENST00000677625.1:c.1217A>C	ENSP00000502857.1:p.Asp406Ala
ENST00000677856.1:n.1524A>C
ENST00000677915.1:c.*168A>C	ENSP00000503118.1:n.*168A>C
ENST00000678533.1:c.*825A>C	ENSP00000503873.1:n.*825A>C
ENST00000678592.1:c.*211A>C	ENSP00000504424.1:n.*211A>C
ENST00000278407.8:c.1271A>C	ENSP00000278407.4:p.Asp424Ala
ENST00000340687.10:c.1160A>C	ENSP00000341861.6:p.Asp387Ala
ENST00000378323.8:c.1286A>C	ENSP00000367574.4:p.Asp429Ala
ENST00000378324.6:c.1115A>C	ENSP00000367575.2:p.Asp372Ala
ENST00000403558.1:c.1400A>C	ENSP00000384420.1:p.Asp467Ala
ENST00000528996.1:c.472A>C	ENSP00000431226.1:n.472A>C
ENST00000530113.1:n.728A>C
ENST00000531133.5:c.772A>C	ENSP00000435431.1:n.772A>C
ENST00000531797.5:c.*296A>C	ENSP00000432554.1:n.*296A>C
ENST00000619430.1:c.402A>C	ENSP00000478572.1:p.Ter134Cys
NM_000062.2:c.1271A>C , LRG_105t1:c.1271A>C	NP_000053.2:p.Asp424Ala
NM_001032295.1:c.1271A>C	NP_001027466.1:p.Asp424Ala
NM_000062.3:c.1271A>C MANE Select	NP_000053.2:p.Asp424Ala
NM_001032295.2:c.1271A>C	NP_001027466.1:p.Asp424Ala