Canonical Allele Identifier: CA2639263345
Gene: ACE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63487070_63487076dup , CM000679.2:g.63487070_63487076dup GRCh38
NC_000017.10:g.61564431_61564437dup , CM000679.1:g.61564431_61564437dup GRCh37
NC_000017.9:g.58918163_58918169dup NCBI36
NG_011648.1:g.14998_15004dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000290866.10:c.2302_2305+3dup
ENST00000290863.10:c.580_583+3dup
ENST00000290866.9:c.2302_2305+3dup
ENST00000413513.7:c.580_583+3dup
ENST00000428043.5:c.2302_2305+3dup
ENST00000577647.2:c.580_583+3dup
ENST00000578839.5:c.*372_*375+3dup
ENST00000579204.1:c.483_486+3dup
ENST00000579314.5:c.580_583+3dup
ENST00000582005.5:c.*222_*225+3dup
ENST00000582761.1:c.70_73+3dup
ENST00000584865.5:n.248_251+3dup
NM_000789.3:c.2302_2305+3dup
NM_001178057.1:c.580_583+3dup
NM_152830.2:c.580_583+3dup
XM_005257110.1:c.1753_1756+3dup
XM_006721737.2:c.640_643+3dup
XM_006721737.3:c.640_643+3dup
NM_000789.4:c.2302_2305+3dup
NM_001178057.2:c.580_583+3dup
NM_152830.3:c.580_583+3dup
NM_001382700.1:c.1735_1738+3dup
NM_001382701.1:c.1450_1453+3dup
NM_001382702.1:c.232_235+3dup
NR_168483.1:n.602_605+3dup