Canonical Allele Identifier: CA381448011

Gene: ACTN3

Linked Data

• gnomAD v4: 11-66560729-C-T
• MyVariant Identifiers: chr11:g.66328200C>T (hg19) ; chr11:g.66560729C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66560729C>T , CM000673.2:g.66560729C>T	GRCh38
NC_000011.9:g.66328200C>T , CM000673.1:g.66328200C>T	GRCh37
NC_000011.8:g.66084776C>T	NCBI36
NG_013304.2:g.18810C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513398.2:c.1834C>T MANE Select	ENSP00000426797.1:p.Gln612Ter
ENST00000502692.5:c.1963C>T	ENSP00000422007.1:p.Gln655Ter
ENST00000513398.1:c.1834C>T	ENSP00000426797.1:p.Gln612Ter
NM_001104.3:c.1834C>T	NP_001095.2:p.Gln612Ter
NM_001258371.2:c.1963C>T	NP_001245300.2:p.Gln655Ter
NM_001104.4:c.1834C>T MANE Select	NP_001095.2:p.Gln612Ter
NM_001258371.3:c.1963C>T	NP_001245300.2:p.Gln655Ter