Canonical Allele Identifier: CA527299894

Gene: SERPINC1

Linked Data

• dbSNP Id: rs1315296013
• gnomAD v2: 1-173880397-TGCAGGTTATATGGGGTTG-T
• gnomAD v3: 1-173911259-TGCAGGTTATATGGGGTTG-T
• gnomAD v4: 1-173911259-TGCAGGTTATATGGGGTTG-T
• MyVariant Identifiers: chr1:g.173880398_173880415del (hg19) ; chr1:g.173911260_173911277del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173911291_173911308del , CM000663.2:g.173911291_173911308del	GRCh38
NC_000001.10:g.173880429_173880446del , CM000663.1:g.173880429_173880446del	GRCh37
NC_000001.9:g.172147052_172147069del	NCBI36
NG_012462.1:g.11102_11119del , LRG_577:g.11102_11119del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.625-386_625-369del MANE Select	ENSP00000356671.3:n.625-386_625-369del
ENST00000367698.3:c.625-386_625-369del	ENSP00000356671.3:n.625-386_625-369del
ENST00000487183.1:n.330-440_330-423del
ENST00000617423.4:c.559+587_559+604del	ENSP00000478688.1:n.559+587_559+604del
NM_000488.3:c.625-386_625-369del , LRG_577t1:c.625-386_625-369del	NP_000479.1:n.625-386_625-369del
XM_005245198.2:c.481-386_481-369del	XP_005245255.1:n.481-386_481-369del
NM_001365052.1:c.481-386_481-369del	NP_001351981.1:n.481-386_481-369del
NM_000488.4:c.625-386_625-369del MANE Select	NP_000479.1:n.625-386_625-369del
NM_001365052.2:c.481-386_481-369del	NP_001351981.1:n.481-386_481-369del
NM_001386302.1:c.625-386_625-369del	NP_001373231.1:n.625-386_625-369del
NM_001386303.1:c.706-386_706-369del	NP_001373232.1:n.706-386_706-369del
NM_001386304.1:c.625-386_625-369del	NP_001373233.1:n.625-386_625-369del
NM_001386305.1:c.625-386_625-369del	NP_001373234.1:n.625-386_625-369del
NM_001386306.1:c.409-386_409-369del	NP_001373235.1:n.409-386_409-369del