Canonical Allele Identifier: CA1975531668

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606254_57606257delinsCCTT , CM000673.2:g.57606254_57606257delinsCCTT	GRCh38
NC_000011.9:g.57373727_57373730delinsCCTT , CM000673.1:g.57373727_57373730delinsCCTT	GRCh37
NC_000011.8:g.57130303_57130306delinsCCTT	NCBI36
NG_009625.1:g.13701_13704delinsCCTT , LRG_105:g.13701_13704delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.889+41_889+44delinsCCTT MANE Select	ENSP00000278407.4:n.889+41_889+44delinsCCTT
ENST00000528996.2:c.59-5472_59-5469delinsCCTT	ENSP00000431226.2:n.59-5472_59-5469delinsCCTT
ENST00000531605.2:c.*665+41_*665+44delinsCCTT	ENSP00000503752.1:n.*665+41_*665+44delinsCCTT
ENST00000619430.2:c.686-154_686-151delinsCCTT	ENSP00000478572.2:n.686-154_686-151delinsCCTT
ENST00000676670.1:c.889+41_889+44delinsCCTT	ENSP00000504807.1:n.889+41_889+44delinsCCTT
ENST00000676741.1:n.1971+41_1971+44delinsCCTT
ENST00000677624.1:c.*309+41_*309+44delinsCCTT	ENSP00000503979.1:n.*309+41_*309+44delinsCCTT
ENST00000677625.1:c.889+41_889+44delinsCCTT	ENSP00000502857.1:n.889+41_889+44delinsCCTT
ENST00000677856.1:n.989_992delinsCCTT
ENST00000677915.1:c.685+4085_685+4088delinsCCTT	ENSP00000503118.1:n.685+4085_685+4088delinsCCTT
ENST00000678533.1:c.*443+41_*443+44delinsCCTT	ENSP00000503873.1:n.*443+41_*443+44delinsCCTT
ENST00000678592.1:c.889+41_889+44delinsCCTT	ENSP00000504424.1:n.889+41_889+44delinsCCTT
ENST00000278407.8:c.889+41_889+44delinsCCTT	ENSP00000278407.4:n.889+41_889+44delinsCCTT
ENST00000340687.10:c.889+41_889+44delinsCCTT	ENSP00000341861.6:n.889+41_889+44delinsCCTT
ENST00000378323.8:c.904+41_904+44delinsCCTT	ENSP00000367574.4:n.904+41_904+44delinsCCTT
ENST00000378324.6:c.733+41_733+44delinsCCTT	ENSP00000367575.2:n.733+41_733+44delinsCCTT
ENST00000403558.1:c.991+41_991+44delinsCCTT	ENSP00000384420.1:n.991+41_991+44delinsCCTT
ENST00000531133.5:c.390+41_390+44delinsCCTT	ENSP00000435431.1:n.390+41_390+44delinsCCTT
ENST00000531797.5:c.*54+4085_*54+4088delinsCCTT	ENSP00000432554.1:n.*54+4085_*54+4088delinsCCTT
ENST00000619430.1:c.349-5651_349-5648delinsCCTT	ENSP00000478572.1:n.349-5651_349-5648delinsCCTT
NM_000062.2:c.889+41_889+44delinsCCTT , LRG_105t1:c.889+41_889+44delinsCCTT	NP_000053.2:n.889+41_889+44delinsCCTT
NM_001032295.1:c.889+41_889+44delinsCCTT	NP_001027466.1:n.889+41_889+44delinsCCTT
NM_000062.3:c.889+41_889+44delinsCCTT MANE Select	NP_000053.2:n.889+41_889+44delinsCCTT
NM_001032295.2:c.889+41_889+44delinsCCTT	NP_001027466.1:n.889+41_889+44delinsCCTT