Canonical Allele Identifier: CA400557840

Gene: ACE

Linked Data

• MyVariant Identifiers: chr17:g.61566038A>C (hg19) ; chr17:g.63488677A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488677A>C , CM000679.2:g.63488677A>C	GRCh38
NC_000017.10:g.61566038A>C , CM000679.1:g.61566038A>C	GRCh37
NC_000017.9:g.58919770A>C	NCBI36
NG_011648.1:g.16605A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000290866.10:c.2335A>C MANE Select	ENSP00000290866.4:p.Lys779Gln
ENST00000290863.10:c.613A>C	ENSP00000290863.6:p.Lys205Gln
ENST00000290866.9:c.2335A>C	ENSP00000290866.4:p.Lys779Gln
ENST00000413513.7:c.613A>C	ENSP00000392247.3:p.Lys205Gln
ENST00000428043.5:c.2335A>C	ENSP00000397593.2:p.Lys779Gln
ENST00000577647.2:c.613A>C	ENSP00000464149.1:p.Lys205Gln
ENST00000578839.5:c.*405A>C	ENSP00000462110.2:n.*405A>C
ENST00000579204.1:c.594A>C	ENSP00000464629.1:n.594A>C
ENST00000579314.5:c.*64A>C	ENSP00000462599.1:n.*64A>C
ENST00000582005.5:c.*255A>C	ENSP00000462002.1:n.*255A>C
ENST00000582761.1:c.103A>C	ENSP00000462909.1:p.Lys35Gln
ENST00000584865.5:n.281A>C
NM_000789.3:c.2335A>C	NP_000780.1:p.Lys779Gln
NM_001178057.1:c.613A>C	NP_001171528.1:p.Lys205Gln
NM_152830.2:c.613A>C	NP_690043.1:p.Lys205Gln
XM_005257110.1:c.1786A>C	XP_005257167.1:p.Lys596Gln
XM_006721737.2:c.673A>C	XP_006721800.2:p.Lys225Gln
XM_006721737.3:c.673A>C	XP_006721800.2:p.Lys225Gln
NM_000789.4:c.2335A>C MANE Select	NP_000780.1:p.Lys779Gln
NM_001178057.2:c.613A>C	NP_001171528.1:p.Lys205Gln
NM_152830.3:c.613A>C	NP_690043.1:p.Lys205Gln
NM_001382700.1:c.1768A>C	NP_001369629.1:p.Lys590Gln
NM_001382701.1:c.1483A>C	NP_001369630.1:p.Lys495Gln
NM_001382702.1:c.265A>C	NP_001369631.1:p.Lys89Gln
NR_168483.1:n.713A>C