Canonical Allele Identifier: CA380699788

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57373678A>T (hg19) ; chr11:g.57606205A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606205A>T , CM000673.2:g.57606205A>T	GRCh38
NC_000011.9:g.57373678A>T , CM000673.1:g.57373678A>T	GRCh37
NC_000011.8:g.57130254A>T	NCBI36
NG_009625.1:g.13652A>T , LRG_105:g.13652A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.881A>T MANE Select	ENSP00000278407.4:p.Tyr294Phe
ENST00000528996.2:c.59-5521A>T	ENSP00000431226.2:n.59-5521A>T
ENST00000531605.2:c.*657A>T	ENSP00000503752.1:n.*657A>T
ENST00000619430.2:c.686-203A>T	ENSP00000478572.2:n.686-203A>T
ENST00000676670.1:c.881A>T	ENSP00000504807.1:p.Tyr294Phe
ENST00000676741.1:n.1963A>T
ENST00000677624.1:c.*301A>T	ENSP00000503979.1:n.*301A>T
ENST00000677625.1:c.881A>T	ENSP00000502857.1:p.Tyr294Phe
ENST00000677856.1:n.940A>T
ENST00000677915.1:c.685+4036A>T	ENSP00000503118.1:n.685+4036A>T
ENST00000678533.1:c.*435A>T	ENSP00000503873.1:n.*435A>T
ENST00000678592.1:c.881A>T	ENSP00000504424.1:p.Tyr294Phe
ENST00000278407.8:c.881A>T	ENSP00000278407.4:p.Tyr294Phe
ENST00000340687.10:c.881A>T	ENSP00000341861.6:p.Tyr294Phe
ENST00000378323.8:c.896A>T	ENSP00000367574.4:p.Tyr299Phe
ENST00000378324.6:c.725A>T	ENSP00000367575.2:p.Tyr242Phe
ENST00000403558.1:c.983A>T	ENSP00000384420.1:p.Tyr328Phe
ENST00000531133.5:c.382A>T	ENSP00000435431.1:n.382A>T
ENST00000531797.5:c.*54+4036A>T	ENSP00000432554.1:n.*54+4036A>T
ENST00000619430.1:c.349-5700A>T	ENSP00000478572.1:n.349-5700A>T
NM_000062.2:c.881A>T , LRG_105t1:c.881A>T	NP_000053.2:p.Tyr294Phe
NM_001032295.1:c.881A>T	NP_001027466.1:p.Tyr294Phe
NM_000062.3:c.881A>T MANE Select	NP_000053.2:p.Tyr294Phe
NM_001032295.2:c.881A>T	NP_001027466.1:p.Tyr294Phe