Canonical Allele Identifier: CA1207937145
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs1657706862

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173910182_173910197del , CM000663.2:g.173910182_173910197del GRCh38
NC_000001.10:g.173879320_173879335del , CM000663.1:g.173879320_173879335del GRCh37
NC_000001.9:g.172145943_172145958del NCBI36
NG_012462.1:g.12187_12202del , LRG_577:g.12187_12202del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.763-250_763-235del MANE Select ENSP00000356671.3:n.763-250_763-235del
ENST00000367698.3:c.763-250_763-235del ENSP00000356671.3:n.763-250_763-235del
ENST00000487183.1:n.414-250_414-235del
ENST00000617423.4:c.559+1672_559+1687del ENSP00000478688.1:n.559+1672_559+1687del
NM_000488.3:c.763-250_763-235del , LRG_577t1:c.763-250_763-235del NP_000479.1:n.763-250_763-235del
XM_005245198.2:c.619-250_619-235del XP_005245255.1:n.619-250_619-235del
NM_001365052.1:c.619-250_619-235del NP_001351981.1:n.619-250_619-235del
NM_000488.4:c.763-250_763-235del MANE Select NP_000479.1:n.763-250_763-235del
NM_001365052.2:c.619-250_619-235del NP_001351981.1:n.619-250_619-235del
NM_001386302.1:c.886-250_886-235del NP_001373231.1:n.886-250_886-235del
NM_001386303.1:c.844-250_844-235del NP_001373232.1:n.844-250_844-235del
NM_001386304.1:c.742-250_742-235del NP_001373233.1:n.742-250_742-235del
NM_001386305.1:c.763-307_763-292del NP_001373234.1:n.763-307_763-292del
NM_001386306.1:c.547-250_547-235del NP_001373235.1:n.547-250_547-235del