Canonical Allele Identifier: CA2269949767

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63496832_63496833delinsCC , CM000679.2:g.63496832_63496833delinsCC	GRCh38
NC_000017.10:g.61574193_61574194delinsCC , CM000679.1:g.61574193_61574194delinsCC	GRCh37
NC_000017.9:g.58927925_58927926delinsCC	NCBI36
NG_011648.1:g.24760_24761delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3538_3539delinsCC MANE Select	ENSP00000290866.4:p.Pro1180=
ENST00000290863.10:c.1816_1817delinsCC	ENSP00000290863.6:p.Pro606=
ENST00000290866.9:c.3538_3539delinsCC	ENSP00000290866.4:p.Pro1180=
ENST00000413513.7:c.1693_1694delinsCC	ENSP00000392247.3:p.Pro565=
ENST00000428043.5:c.3538_3539delinsCC	ENSP00000397593.2:p.Pro1180=
ENST00000577418.5:n.548_549delinsCC
ENST00000577647.2:c.1816_1817delinsCC	ENSP00000464149.1:p.Pro606=
ENST00000578839.5:c.*1293_*1294delinsCC	ENSP00000462110.2:n.*1293_*1294delinsCC
ENST00000579314.5:c.*1267_*1268delinsCC	ENSP00000462599.1:n.*1267_*1268delinsCC
ENST00000579409.1:c.225_226delinsCC
ENST00000582244.1:n.412_413delinsCC
NM_000789.3:c.3538_3539delinsCC	NP_000780.1:p.Pro1180=
NM_001178057.1:c.1693_1694delinsCC	NP_001171528.1:p.Pro565=
NM_152830.2:c.1816_1817delinsCC	NP_690043.1:p.Pro606=
XM_005257110.1:c.2989_2990delinsCC	XP_005257167.1:p.Pro997=
XM_006721737.2:c.1876_1877delinsCC	XP_006721800.2:p.Pro626=
XM_006721737.3:c.1876_1877delinsCC	XP_006721800.2:p.Pro626=
NM_000789.4:c.3538_3539delinsCC MANE Select	NP_000780.1:p.Pro1180=
NM_001178057.2:c.1693_1694delinsCC	NP_001171528.1:p.Pro565=
NM_152830.3:c.1816_1817delinsCC	NP_690043.1:p.Pro606=
NM_001382700.1:c.2971_2972delinsCC	NP_001369629.1:p.Pro991=
NM_001382701.1:c.2686_2687delinsCC	NP_001369630.1:p.Pro896=
NM_001382702.1:c.1153_1154delinsCC	NP_001369631.1:p.Pro385=
NR_168483.1:n.1916_1917delinsCC