Canonical Allele Identifier: CA32780221
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs199469509
MyVariant Identifiers: chr1:g.173878760_173878777del (hg19) chr1:g.173909622_173909639del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909627_173909644del , CM000663.2:g.173909627_173909644del GRCh38
NC_000001.10:g.173878765_173878782del , CM000663.1:g.173878765_173878782del GRCh37
NC_000001.9:g.172145388_172145405del NCBI36
NG_012462.1:g.12740_12757del , LRG_577:g.12740_12757del

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.1066_1083del MANE Select ENSP00000356671.3:p.Arg356_Phe361del
ENST00000367698.3:c.1066_1083del ENSP00000356671.3:p.Arg356_Phe361del
ENST00000617423.4:c.560-2146_560-2129del ENSP00000478688.1:n.560-2146_560-2129del
NM_000488.3:c.1066_1083del , LRG_577t1:c.1066_1083del NP_000479.1:p.Arg356_Phe361del
XM_005245198.2:c.922_939del XP_005245255.1:p.Arg308_Phe313del
NM_001365052.1:c.922_939del NP_001351981.1:p.Arg308_Phe313del
NM_000488.4:c.1066_1083del MANE Select NP_000479.1:p.Arg356_Phe361del
NM_001365052.2:c.922_939del NP_001351981.1:p.Arg308_Phe313del
NM_001386302.1:c.1189_1206del NP_001373231.1:p.Arg397_Phe402del
NM_001386303.1:c.1147_1164del NP_001373232.1:p.Arg383_Phe388del
NM_001386304.1:c.1045_1062del NP_001373233.1:p.Arg349_Phe354del
NM_001386305.1:c.1009_1026del NP_001373234.1:p.Arg337_Phe342del
NM_001386306.1:c.850_867del NP_001373235.1:p.Arg284_Phe289del
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