Canonical Allele Identifier: CA891309447
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs1247393849

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903863_173903866del , CM000663.2:g.173903863_173903866del GRCh38
NC_000001.10:g.173873001_173873004del , CM000663.1:g.173873001_173873004del GRCh37
NC_000001.9:g.172139624_172139627del NCBI36
NG_012462.1:g.18515_18518del , LRG_577:g.18515_18518del

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.*25_*28del MANE Select ENSP00000356671.3:n.*25_*28del
ENST00000367698.3:c.*25_*28del ENSP00000356671.3:n.*25_*28del
ENST00000617423.4:c.*25_*28del ENSP00000478688.1:n.*25_*28del
NM_000488.3:c.*25_*28del , LRG_577t1:c.*25_*28del NP_000479.1:n.*25_*28del
XM_005245198.2:c.*25_*28del XP_005245255.1:n.*25_*28del
NM_001365052.1:c.*25_*28del NP_001351981.1:n.*25_*28del
NM_000488.4:c.*25_*28del MANE Select NP_000479.1:n.*25_*28del
NM_001365052.2:c.*25_*28del NP_001351981.1:n.*25_*28del
NM_001386302.1:c.*25_*28del NP_001373231.1:n.*25_*28del
NM_001386303.1:c.*25_*28del NP_001373232.1:n.*25_*28del
NM_001386304.1:c.*25_*28del NP_001373233.1:n.*25_*28del
NM_001386305.1:c.*25_*28del NP_001373234.1:n.*25_*28del
NM_001386306.1:c.*25_*28del NP_001373235.1:n.*25_*28del