Canonical Allele Identifier: CA2573051419

Gene: SERPINC1

Linked Data

• ClinVar Variation Id: 1321895
• ClinVar RCV Id: RCV001779979

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173908360_173915405del , CM000663.2:g.173908360_173915405del	GRCh38
NC_000001.10:g.173877498_173884543del , CM000663.1:g.173877498_173884543del	GRCh37
NC_000001.9:g.172144121_172151166del	NCBI36
NG_012462.1:g.6974_14019del , LRG_577:g.6974_14019del

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.42-486_1154-846del
ENST00000367698.3:c.42-486_1154-846del
ENST00000617423.4:c.42-486_560-867del
NM_000488.3:c.42-486_1154-846del , LRG_577t1:c.42-486_1154-846del
XM_005245198.2:c.-272-219_1010-846del
NM_001365052.1:c.-272-219_1010-846del
NM_000488.4:c.42-486_1154-846del
NM_001365052.2:c.-272-219_1010-846del
NM_001386302.1:c.42-486_1277-846del
NM_001386303.1:c.123-486_1235-846del
NM_001386304.1:c.42-486_1133-846del
NM_001386305.1:c.42-486_1097-846del
NM_001386306.1:c.42-486_938-846del