Canonical Allele Identifier: CA2269950627

Gene: ACE

Linked Data

• dbSNP Id: rs2030898812

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63498238_63498239insCTCCTC , CM000679.2:g.63498238_63498239insCTCCTC	GRCh38
NC_000017.10:g.61575599_61575600insCTCCTC , CM000679.1:g.61575599_61575600insCTCCTC	GRCh37
NC_000017.9:g.58929331_58929332insCTCCTC	NCBI36
NG_011648.1:g.26166_26167insCTCCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.*872_*873insCTCCTC MANE Select	ENSP00000290866.4:n.*872_*873insCTCCTC
ENST00000290866.9:c.*872_*873insCTCCTC	ENSP00000290866.4:n.*872_*873insCTCCTC
ENST00000428043.5:c.*1215_*1216insCTCCTC	ENSP00000397593.2:n.*1215_*1216insCTCCTC
ENST00000577647.2:c.1969+1253_1969+1254insCTCCTC	ENSP00000464149.1:n.1969+1253_1969+1254insCTCCTC
NM_000789.3:c.*872_*873insCTCCTC	NP_000780.1:n.*872_*873insCTCCTC
NM_001178057.1:c.*872_*873insCTCCTC	NP_001171528.1:n.*872_*873insCTCCTC
NM_152830.2:c.*872_*873insCTCCTC	NP_690043.1:n.*872_*873insCTCCTC
XM_005257110.1:c.*872_*873insCTCCTC	XP_005257167.1:n.*872_*873insCTCCTC
XM_006721737.2:c.*872_*873insCTCCTC	XP_006721800.2:n.*872_*873insCTCCTC
NM_000789.4:c.*872_*873insCTCCTC MANE Select	NP_000780.1:n.*872_*873insCTCCTC
NM_001178057.2:c.*872_*873insCTCCTC	NP_001171528.1:n.*872_*873insCTCCTC
NM_152830.3:c.*872_*873insCTCCTC	NP_690043.1:n.*872_*873insCTCCTC
NM_001382700.1:c.*872_*873insCTCCTC	NP_001369629.1:n.*872_*873insCTCCTC
NM_001382701.1:c.*872_*873insCTCCTC	NP_001369630.1:n.*872_*873insCTCCTC
NM_001382702.1:c.*872_*873insCTCCTC	NP_001369631.1:n.*872_*873insCTCCTC
NR_168483.1:n.3171_3172insCTCCTC