Canonical Allele Identifier: CA2838324842

Gene: CPAMD8

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.16904203_16904205del , CM000681.2:g.16904203_16904205del	GRCh38
NC_000019.9:g.17015013_17015015del , CM000681.1:g.17015013_17015015del	GRCh37
NC_000019.8:g.16876013_16876015del	NCBI36
NG_054892.1:g.127614_127616del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651564.2:c.4251+21_4251+23del	ENSP00000498697.2:n.4251+21_4251+23del
ENST00000682780.1:c.428+21_428+23del
ENST00000443236.7:c.4251+21_4251+23del MANE Select	ENSP00000402505.3:n.4251+21_4251+23del
ENST00000651564.1:c.4392+21_4392+23del	ENSP00000498697.1:n.4392+21_4392+23del
ENST00000388925.8:c.*2107+21_*2107+23del	ENSP00000373577.4:n.*2107+21_*2107+23del
ENST00000443236.5:c.4392+21_4392+23del	ENSP00000402505.2:n.4392+21_4392+23del
NM_015692.2:c.4392+21_4392+23del	NP_056507.2:n.4392+21_4392+23del
XM_011527917.1:c.4356+21_4356+23del	XP_011526219.1:n.4356+21_4356+23del
XM_011527918.1:c.4392+21_4392+23del	XP_011526220.1:n.4392+21_4392+23del
XM_011527919.1:c.4392+21_4392+23del	XP_011526221.1:n.4392+21_4392+23del
XM_011527920.1:c.4392+21_4392+23del	XP_011526222.1:n.4392+21_4392+23del
XM_011527921.1:c.4392+21_4392+23del	XP_011526223.1:n.4392+21_4392+23del
XM_011527922.1:c.4392+21_4392+23del	XP_011526224.1:n.4392+21_4392+23del
XM_011527923.1:c.4392+21_4392+23del	XP_011526225.1:n.4392+21_4392+23del
XM_011527924.1:c.4392+21_4392+23del	XP_011526226.1:n.4392+21_4392+23del
XM_011527925.1:c.2163+21_2163+23del	XP_011526227.1:n.2163+21_2163+23del
NM_015692.4:c.4251+21_4251+23del	NP_056507.3:n.4251+21_4251+23del
XM_011527920.2:c.4392+21_4392+23del	XP_011526222.1:n.4392+21_4392+23del
XM_011527921.3:c.4392+21_4392+23del	XP_011526223.1:n.4392+21_4392+23del
XM_011527924.2:c.4392+21_4392+23del	XP_011526226.1:n.4392+21_4392+23del
XM_017026594.1:c.4392+21_4392+23del	XP_016882083.1:n.4392+21_4392+23del
NM_015692.5:c.4251+21_4251+23del MANE Select	NP_056507.3:n.4251+21_4251+23del