Canonical Allele Identifier: CA400540599

Gene: ACE

Linked Data

• dbSNP Id: rs1221928144
• gnomAD v2: 17-61555311-G-C
• gnomAD v4: 17-63477950-G-C
• MyVariant Identifiers: chr17:g.61555311G>C (hg19) ; chr17:g.63477950G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63477950G>C , CM000679.2:g.63477950G>C	GRCh38
NC_000017.10:g.61555311G>C , CM000679.1:g.61555311G>C	GRCh37
NC_000017.9:g.58909043G>C	NCBI36
NG_011648.1:g.5878G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.269G>C MANE Select	ENSP00000290866.4:p.Ser90Thr
ENST00000290866.9:c.269G>C	ENSP00000290866.4:p.Ser90Thr
ENST00000428043.5:c.269G>C	ENSP00000397593.2:p.Ser90Thr
ENST00000579462.1:n.294G>C
ENST00000580318.1:n.458G>C
ENST00000582627.1:c.269G>C	ENSP00000462280.1:p.Ser90Thr
ENST00000582678.5:c.269G>C	ENSP00000462995.1:p.Ser90Thr
ENST00000583336.5:n.303G>C
ENST00000584529.5:n.303G>C
NM_000789.3:c.269G>C	NP_000780.1:p.Ser90Thr
XM_005257110.1:c.-187G>C	XP_005257167.1:n.-187G>C
NM_000789.4:c.269G>C MANE Select	NP_000780.1:p.Ser90Thr
NM_001382700.1:c.34G>C	NP_001369629.1:p.Ala12Pro
NM_001382701.1:c.-346G>C	NP_001369630.1:n.-346G>C