Canonical Allele Identifier: CA1207937835

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173911935_173911937delinsTAG , CM000663.2:g.173911935_173911937delinsTAG	GRCh38
NC_000001.10:g.173881073_173881075delinsTAG , CM000663.1:g.173881073_173881075delinsTAG	GRCh37
NC_000001.9:g.172147696_172147698delinsTAG	NCBI36
NG_012462.1:g.10442_10444delinsCTA , LRG_577:g.10442_10444delinsCTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.486_488delinsCTA MANE Select	ENSP00000356671.3:p.Leu162=
ENST00000367698.3:c.486_488delinsCTA	ENSP00000356671.3:p.Leu162=
ENST00000487183.1:n.191_193delinsCTA
ENST00000617423.4:c.486_488delinsCTA	ENSP00000478688.1:p.Leu162=
NM_000488.3:c.486_488delinsCTA , LRG_577t1:c.486_488delinsCTA	NP_000479.1:p.Leu162=
XM_005245198.2:c.342_344delinsCTA	XP_005245255.1:p.Leu114=
NM_001365052.1:c.342_344delinsCTA	NP_001351981.1:p.Leu114=
NM_000488.4:c.486_488delinsCTA MANE Select	NP_000479.1:p.Leu162=
NM_001365052.2:c.342_344delinsCTA	NP_001351981.1:p.Leu114=
NM_001386302.1:c.486_488delinsCTA	NP_001373231.1:p.Leu162=
NM_001386303.1:c.567_569delinsCTA	NP_001373232.1:p.Leu189=
NM_001386304.1:c.486_488delinsCTA	NP_001373233.1:p.Leu162=
NM_001386305.1:c.486_488delinsCTA	NP_001373234.1:p.Leu162=
NM_001386306.1:c.409-1046_409-1044delinsCTA	NP_001373235.1:n.409-1046_409-1044delinsC...