Canonical Allele Identifier: CA343772365

Gene: SERPINC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903969G>A , CM000663.2:g.173903969G>A	GRCh38
NC_000001.10:g.173873107G>A , CM000663.1:g.173873107G>A	GRCh37
NC_000001.9:g.172139730G>A	NCBI36
NG_012462.1:g.18410C>T , LRG_577:g.18410C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000488.4:c.1315C>T MANE Select	NP_000479.1:p.Pro439Ser
ENST00000367698.4:c.1315C>T MANE Select	ENSP00000356671.3:p.Pro439Ser
NM_000488.3:c.1315C>T , LRG_577t1:c.1315C>T	NP_000479.1:p.Pro439Ser
NM_001365052.1:c.1171C>T	NP_001351981.1:p.Pro391Ser
NM_001365052.2:c.1171C>T	NP_001351981.1:p.Pro391Ser
NM_001386302.1:c.1438C>T	NP_001373231.1:p.Pro480Ser
NM_001386303.1:c.1396C>T	NP_001373232.1:p.Pro466Ser
NM_001386304.1:c.1294C>T	NP_001373233.1:p.Pro432Ser
NM_001386305.1:c.1258C>T	NP_001373234.1:p.Pro420Ser
NM_001386306.1:c.1099C>T	NP_001373235.1:p.Pro367Ser
ENST00000367698.3:c.1315C>T	ENSP00000356671.3:p.Pro439Ser
ENST00000617423.4:c.700C>T	ENSP00000478688.1:p.Pro234Ser
XM_005245198.2:c.1171C>T	XP_005245255.1:p.Pro391Ser