Canonical Allele Identifier: CA343773594

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878751C>G (hg19) ; chr1:g.173909613C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909613C>G , CM000663.2:g.173909613C>G	GRCh38
NC_000001.10:g.173878751C>G , CM000663.1:g.173878751C>G	GRCh37
NC_000001.9:g.172145374C>G	NCBI36
NG_012462.1:g.12766G>C , LRG_577:g.12766G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1092G>C MANE Select	ENSP00000356671.3:p.Lys364Asn
ENST00000367698.3:c.1092G>C	ENSP00000356671.3:p.Lys364Asn
ENST00000617423.4:c.560-2120G>C	ENSP00000478688.1:n.560-2120G>C
NM_000488.3:c.1092G>C , LRG_577t1:c.1092G>C	NP_000479.1:p.Lys364Asn
XM_005245198.2:c.948G>C	XP_005245255.1:p.Lys316Asn
NM_001365052.1:c.948G>C	NP_001351981.1:p.Lys316Asn
NM_000488.4:c.1092G>C MANE Select	NP_000479.1:p.Lys364Asn
NM_001365052.2:c.948G>C	NP_001351981.1:p.Lys316Asn
NM_001386302.1:c.1215G>C	NP_001373231.1:p.Lys405Asn
NM_001386303.1:c.1173G>C	NP_001373232.1:p.Lys391Asn
NM_001386304.1:c.1071G>C	NP_001373233.1:p.Lys357Asn
NM_001386305.1:c.1035G>C	NP_001373234.1:p.Lys345Asn
NM_001386306.1:c.876G>C	NP_001373235.1:p.Lys292Asn