Canonical Allele Identifier: CA2740090406

Gene: SERPINC1

Linked Data

• ClinVar Variation Id: 2978886
• ClinVar RCV Id: RCV003839532

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909545G>A , CM000663.2:g.173909545G>A	GRCh38
NC_000001.10:g.173878683G>A , CM000663.1:g.173878683G>A	GRCh37
NC_000001.9:g.172145306G>A	NCBI36
NG_012462.1:g.12834C>T , LRG_577:g.12834C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1153+7C>T MANE Select	ENSP00000356671.3:n.1153+7C>T
ENST00000367698.3:c.1153+7C>T	ENSP00000356671.3:n.1153+7C>T
ENST00000617423.4:c.560-2052C>T	ENSP00000478688.1:n.560-2052C>T
NM_000488.3:c.1153+7C>T , LRG_577t1:c.1153+7C>T	NP_000479.1:n.1153+7C>T
XM_005245198.2:c.1009+7C>T	XP_005245255.1:n.1009+7C>T
NM_001365052.1:c.1009+7C>T	NP_001351981.1:n.1009+7C>T
NM_000488.4:c.1153+7C>T MANE Select	NP_000479.1:n.1153+7C>T
NM_001365052.2:c.1009+7C>T	NP_001351981.1:n.1009+7C>T
NM_001386302.1:c.1276+7C>T	NP_001373231.1:n.1276+7C>T
NM_001386303.1:c.1234+7C>T	NP_001373232.1:n.1234+7C>T
NM_001386304.1:c.1132+7C>T	NP_001373233.1:n.1132+7C>T
NM_001386305.1:c.1096+7C>T	NP_001373234.1:n.1096+7C>T
NM_001386306.1:c.937+7C>T	NP_001373235.1:n.937+7C>T