Canonical Allele Identifier: CA170975

Gene: SERPINB7

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.63798671dup , CM000680.2:g.63798671dup	GRCh38
NC_000018.9:g.61465905dup , CM000680.1:g.61465905dup	GRCh37
NC_000018.8:g.59616885dup	NCBI36
NG_034150.1:g.50625dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398019.7:c.522dup MANE Select	ENSP00000381101.2:p.Val175CysfsTer?
ENST00000336429.6:c.522dup	ENSP00000337212.2:p.Val175CysfsTer?
ENST00000398019.6:c.522dup	ENSP00000381101.2:p.Val175CysfsTer?
ENST00000540675.5:c.471dup	ENSP00000444572.1:p.Val158CysfsTer?
ENST00000546027.5:c.522dup	ENSP00000444861.1:p.Val175CysfsTer?
NM_001040147.2:c.522dup	NP_001035237.1:p.Val175CysfsTer?
NM_001261830.1:c.522dup	NP_001248759.1:p.Val175CysfsTer?
NM_001261831.1:c.471dup	NP_001248760.1:p.Val158CysfsTer?
NM_003784.3:c.522dup	NP_003775.1:p.Val175CysfsTer?
XM_006722562.1:c.522dup	XP_006722625.1:p.Val175CysfsTer?
XM_011526236.1:c.522dup	XP_011524538.1:p.Val175CysfsTer?
XM_024451278.1:c.522dup	XP_024307046.1:p.Val175CysfsTer?
NM_003784.4:c.522dup MANE Select	NP_003775.1:p.Val175CysfsTer?
NM_001040147.3:c.522dup	NP_001035237.1:p.Val175CysfsTer?
NM_001261830.2:c.522dup	NP_001248759.1:p.Val175CysfsTer?
NM_001261831.2:c.471dup	NP_001248760.1:p.Val158CysfsTer?