Canonical Allele Identifier: CA366703505

Gene: ACTB

Linked Data

• MyVariant Identifiers: chr7:g.5568245C>G (hg19) ; chr7:g.5528614C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528614C>G , CM000669.2:g.5528614C>G	GRCh38
NC_000007.13:g.5568245C>G , CM000669.1:g.5568245C>G	GRCh37
NC_000007.12:g.5534771C>G	NCBI36
NG_007992.1:g.6988G>C , LRG_132:g.6988G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000432588.6:c.469G>C	ENSP00000407473.2:p.Asp157His
ENST00000473257.3:c.340G>C	ENSP00000501773.1:p.Asp114His
ENST00000477812.2:n.1016G>C
ENST00000493945.6:c.469G>C	ENSP00000494269.1:p.Asp157His
ENST00000642480.2:c.469G>C	ENSP00000495995.2:p.Asp157His
ENST00000645576.1:c.421G>C	ENSP00000496101.1:p.Asp141His
ENST00000646664.1:c.469G>C MANE Select	ENSP00000494750.1:p.Asp157His
ENST00000647275.1:c.103G>C	ENSP00000494185.1:p.Asp35His
ENST00000674681.1:c.469G>C	ENSP00000502821.1:p.Asp157His
ENST00000675515.1:c.469G>C	ENSP00000501862.1:p.Asp157His
ENST00000676189.1:c.*12G>C	ENSP00000502538.1:n.*12G>C
ENST00000676319.1:c.88-831G>C	ENSP00000502193.1:n.88-831G>C
ENST00000676397.1:c.469G>C	ENSP00000502286.1:p.Asp157His
ENST00000331789.9:c.469G>C	ENSP00000349960.4:p.Asp157His
ENST00000425660.5:c.*132G>C	ENSP00000409264.1:n.*132G>C
ENST00000432588.5:c.469G>C	ENSP00000407473.1:p.Asp157His
ENST00000462494.5:n.994G>C
ENST00000473257.1:n.187G>C
ENST00000477812.1:n.676G>C
ENST00000484841.5:n.624G>C
ENST00000493945.5:n.475G>C
NM_001101.3:c.469G>C , LRG_132t1:c.469G>C	NP_001092.1:p.Asp157His
XM_006715764.1:c.103G>C	XP_006715827.1:p.Asp35His
NM_001101.4:c.469G>C	NP_001092.1:p.Asp157His
NM_001101.5:c.469G>C MANE Select	NP_001092.1:p.Asp157His