Canonical Allele Identifier: CA2649173925

Gene: SERPINC1

Linked Data

• gnomAD v4: 1-173909549-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909549A>C , CM000663.2:g.173909549A>C	GRCh38
NC_000001.10:g.173878687A>C , CM000663.1:g.173878687A>C	GRCh37
NC_000001.9:g.172145310A>C	NCBI36
NG_012462.1:g.12830T>G , LRG_577:g.12830T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1153+3T>G MANE Select	ENSP00000356671.3:n.1153+3T>G
ENST00000367698.3:c.1153+3T>G	ENSP00000356671.3:n.1153+3T>G
ENST00000617423.4:c.560-2056T>G	ENSP00000478688.1:n.560-2056T>G
NM_000488.3:c.1153+3T>G , LRG_577t1:c.1153+3T>G	NP_000479.1:n.1153+3T>G
XM_005245198.2:c.1009+3T>G	XP_005245255.1:n.1009+3T>G
NM_001365052.1:c.1009+3T>G	NP_001351981.1:n.1009+3T>G
NM_000488.4:c.1153+3T>G MANE Select	NP_000479.1:n.1153+3T>G
NM_001365052.2:c.1009+3T>G	NP_001351981.1:n.1009+3T>G
NM_001386302.1:c.1276+3T>G	NP_001373231.1:n.1276+3T>G
NM_001386303.1:c.1234+3T>G	NP_001373232.1:n.1234+3T>G
NM_001386304.1:c.1132+3T>G	NP_001373233.1:n.1132+3T>G
NM_001386305.1:c.1096+3T>G	NP_001373234.1:n.1096+3T>G
NM_001386306.1:c.937+3T>G	NP_001373235.1:n.937+3T>G