Canonical Allele Identifier: CA345373471

Gene: ACTN2

Linked Data

• MyVariant Identifiers: chr1:g.236882206C>G (hg19) ; chr1:g.236718906C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236718906C>G , CM000663.2:g.236718906C>G	GRCh38
NC_000001.10:g.236882206C>G , CM000663.1:g.236882206C>G	GRCh37
NC_000001.9:g.234948829C>G	NCBI36
NG_009081.1:g.37437C>G
NG_009081.2:g.59766C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.254C>G	ENSP00000443495.1:p.Pro85Arg
ENST00000492634.7:n.349C>G
ENST00000494762.2:n.3C>G
ENST00000682015.1:c.254C>G	ENSP00000506961.1:p.Pro85Arg
ENST00000682692.1:n.254C>G
ENST00000682966.1:n.253C>G
ENST00000683075.1:n.193C>G
ENST00000683111.1:c.197C>G	ENSP00000507913.1:p.Pro66Arg
ENST00000684050.1:n.289C>G
ENST00000684286.1:n.322C>G
ENST00000684502.1:n.289C>G
ENST00000366578.6:c.254C>G MANE Select	ENSP00000355537.4:p.Pro85Arg
ENST00000492634.6:n.349C>G
ENST00000542672.6:c.254C>G	ENSP00000443495.1:p.Pro85Arg
ENST00000651091.1:c.197C>G	ENSP00000498677.1:p.Pro66Arg
ENST00000651187.1:c.38C>G	ENSP00000498348.1:p.Pro13Arg
ENST00000651275.1:c.239C>G	ENSP00000498926.1:p.Pro80Arg
ENST00000651786.1:c.254C>G	ENSP00000498364.1:p.Pro85Arg
ENST00000652096.1:c.254C>G	ENSP00000498896.1:p.Pro85Arg
ENST00000366578.5:c.254C>G	ENSP00000355537.4:p.Pro85Arg
ENST00000492634.5:n.401C>G
ENST00000542672.5:c.254C>G	ENSP00000443495.1:p.Pro85Arg
ENST00000546208.5:c.-568C>G	ENSP00000438384.2:n.-568C>G
NM_001103.3:c.254C>G	NP_001094.1:p.Pro85Arg
NM_001278343.1:c.254C>G	NP_001265272.1:p.Pro85Arg
NM_001278344.1:c.-568C>G	NP_001265273.1:n.-568C>G
NM_001278343.2:c.254C>G	NP_001265272.1:p.Pro85Arg
NM_001103.4:c.254C>G MANE Select	NP_001094.1:p.Pro85Arg
NM_001278344.2:c.-568C>G	NP_001265273.1:n.-568C>G