Canonical Allele Identifier: CA476740623

Gene: CASP5

Linked Data

• gnomAD v4: 11-105007096-G-A
• MyVariant Identifiers: chr11:g.104877823G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.105007096G>A , CM000673.2:g.105007096G>A	GRCh38
NC_000011.9:g.104877823G>A , CM000673.1:g.104877823G>A	GRCh37
NC_000011.8:g.104383033G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000260315.8:c.420C>T MANE Select	ENSP00000260315.3:p.Ile140=
ENST00000260315.7:c.420C>T	ENSP00000260315.3:p.Ile140=
ENST00000393141.6:c.459C>T	ENSP00000376849.2:p.Ile153=
ENST00000418434.5:c.8-3713C>T	ENSP00000398130.1:n.8-3713C>T
ENST00000444749.6:c.246C>T	ENSP00000388365.2:p.Ile82=
ENST00000456094.1:c.372C>T	ENSP00000415241.1:p.Ile124=
ENST00000456200.5:c.246C>T	ENSP00000408455.1:p.Ile82=
ENST00000526056.5:c.459C>T	ENSP00000436877.1:p.Ile153=
ENST00000531367.5:c.8-3713C>T	ENSP00000434471.1:n.8-3713C>T
NM_001136109.1:c.246C>T	NP_001129581.1:p.Ile82=
NM_001136110.1:c.8-3713C>T	NP_001129582.1:n.8-3713C>T
NM_001136112.1:c.459C>T	NP_001129584.1:p.Ile153=
NM_004347.3:c.420C>T	NP_004338.3:p.Ile140=
NR_024239.1:n.278C>T
NR_036562.1:n.40-4895C>T
XM_011543020.1:c.181+1711C>T	XP_011541322.1:n.181+1711C>T
XM_011543021.1:c.420C>T	XP_011541323.1:p.Ile140=
NM_001136109.2:c.246C>T	NP_001129581.1:p.Ile82=
NM_001136110.2:c.8-3713C>T	NP_001129582.1:n.8-3713C>T
NM_001136112.2:c.459C>T	NP_001129584.1:p.Ile153=
NM_004347.4:c.420C>T	NP_004338.3:p.Ile140=
NR_024239.2:n.278C>T
NR_036562.2:n.40-4895C>T
XM_011543021.2:c.420C>T	XP_011541323.1:p.Ile140=
NM_004347.5:c.420C>T MANE Select	NP_004338.3:p.Ile140=
NM_001136109.3:c.246C>T	NP_001129581.1:p.Ile82=
NM_001136110.3:c.8-3713C>T	NP_001129582.1:n.8-3713C>T
NM_001136112.3:c.459C>T	NP_001129584.1:p.Ile153=
NR_024239.3:n.278C>T
NR_036562.3:n.40-4895C>T