Canonical Allele Identifier: CA2580061384

Gene: SERPINC1

Linked Data

• ClinVar Variation Id: 1954374
• ClinVar RCV Id: RCV002715013
• ERepo: CA2580061384/MONDO:0013144/084

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904073T>C , CM000663.2:g.173904073T>C	GRCh38
NC_000001.10:g.173873211T>C , CM000663.1:g.173873211T>C	GRCh37
NC_000001.9:g.172139834T>C	NCBI36
NG_012462.1:g.18306A>G , LRG_577:g.18306A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1219-8A>G MANE Select	ENSP00000356671.3:n.1219-8A>G
ENST00000367698.3:c.1219-8A>G	ENSP00000356671.3:n.1219-8A>G
ENST00000617423.4:c.604-8A>G	ENSP00000478688.1:n.604-8A>G
NM_000488.3:c.1219-8A>G , LRG_577t1:c.1219-8A>G	NP_000479.1:n.1219-8A>G
XM_005245198.2:c.1075-8A>G	XP_005245255.1:n.1075-8A>G
NM_001365052.1:c.1075-8A>G	NP_001351981.1:n.1075-8A>G
NM_000488.4:c.1219-8A>G MANE Select	NP_000479.1:n.1219-8A>G
NM_001365052.2:c.1075-8A>G	NP_001351981.1:n.1075-8A>G
NM_001386302.1:c.1342-8A>G	NP_001373231.1:n.1342-8A>G
NM_001386303.1:c.1300-8A>G	NP_001373232.1:n.1300-8A>G
NM_001386304.1:c.1198-8A>G	NP_001373233.1:n.1198-8A>G
NM_001386305.1:c.1162-8A>G	NP_001373234.1:n.1162-8A>G
NM_001386306.1:c.1003-8A>G	NP_001373235.1:n.1003-8A>G