Canonical Allele Identifier: CA501341480

Gene: ACE

Linked Data

• gnomAD v4: 17-63478002-G-T
• MyVariant Identifiers: chr17:g.61555363G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63478002G>T , CM000679.2:g.63478002G>T	GRCh38
NC_000017.10:g.61555363G>T , CM000679.1:g.61555363G>T	GRCh37
NC_000017.9:g.58909095G>T	NCBI36
NG_011648.1:g.5930G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.321G>T MANE Select	ENSP00000290866.4:p.Pro107=
ENST00000290866.9:c.321G>T	ENSP00000290866.4:p.Pro107=
ENST00000428043.5:c.321G>T	ENSP00000397593.2:p.Pro107=
ENST00000579462.1:n.346G>T
ENST00000580318.1:n.510G>T
ENST00000582627.1:c.321G>T	ENSP00000462280.1:p.Pro107=
ENST00000582678.5:c.321G>T	ENSP00000462995.1:p.Pro107=
ENST00000583336.5:n.355G>T
ENST00000584529.5:n.355G>T
NM_000789.3:c.321G>T	NP_000780.1:p.Pro107=
XM_005257110.1:c.-135G>T	XP_005257167.1:n.-135G>T
NM_000789.4:c.321G>T MANE Select	NP_000780.1:p.Pro107=
NM_001382700.1:c.86G>T	NP_001369629.1:p.Arg29Leu
NM_001382701.1:c.-294G>T	NP_001369630.1:n.-294G>T