Canonical Allele Identifier: CA2416989880

Gene: ACE2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.15599938A= , CM000685.2:g.15599938A=	GRCh38
NC_000023.10:g.15618061A= , CM000685.1:g.15618061A=	GRCh37
NC_000023.9:g.15527982A=	NCBI36
NG_012575.1:g.7132T=
NG_012575.2:g.7221T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001371415.1:c.186+788T= MANE Select	NP_001358344.1:n.186+788T=
ENST00000252519.8:c.186+788T= MANE Select	ENSP00000252519.3:n.186+788T=
NM_001386259.1:c.186+788T=	NP_001373188.1:n.186+788T=
NM_001386260.1:c.186+788T=	NP_001373189.1:n.186+788T=
NM_001389402.1:c.186+788T=	NP_001376331.1:n.186+788T=
NM_021804.2:c.186+788T=	NP_068576.1:n.186+788T=
NM_021804.3:c.186+788T=	NP_068576.1:n.186+788T=
ENST00000252519.7:c.186+788T=	ENSP00000252519.3:n.186+788T=
ENST00000427411.1:c.186+788T=	ENSP00000389326.1:n.186+788T=
ENST00000427411.2:c.186+788T=	ENSP00000389326.1:n.186+788T=
ENST00000484756.1:n.482+788T=
ENST00000649243.1:c.*264+788T=	ENSP00000497489.1:n.*264+788T=
ENST00000678046.1:c.186+788T=	ENSP00000502872.1:n.186+788T=
ENST00000678073.1:c.186+788T=	ENSP00000504103.1:n.186+788T=
ENST00000679162.1:c.186+788T=	ENSP00000503771.1:n.186+788T=
ENST00000679212.1:c.186+788T=	ENSP00000503558.1:n.186+788T=
ENST00000679278.1:c.186+788T=	ENSP00000504010.1:n.186+788T=
ENST00000680121.1:c.186+788T=	ENSP00000505992.1:n.186+788T=
XM_011545549.1:c.186+788T=	XP_011543851.1:n.186+788T=
XM_011545549.2:c.186+788T=	XP_011543851.1:n.186+788T=
XM_011545550.1:c.186+788T=	XP_011543852.1:n.186+788T=
XM_011545551.1:c.186+788T=	XP_011543853.1:n.186+788T=
XM_011545551.3:c.186+788T=	XP_011543853.1:n.186+788T=
XM_011545552.1:c.186+788T=	XP_011543854.1:n.186+788T=
XM_011545552.2:c.186+788T=	XP_011543854.1:n.186+788T=