Canonical Allele Identifier: CA366702021

Gene: ACTB

Linked Data

• MyVariant Identifiers: chr7:g.5567996A>G (hg19) ; chr7:g.5528365A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528365A>G , CM000669.2:g.5528365A>G	GRCh38
NC_000007.13:g.5567996A>G , CM000669.1:g.5567996A>G	GRCh37
NC_000007.12:g.5534522A>G	NCBI36
NG_007992.1:g.7237T>C , LRG_132:g.7237T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000432588.6:c.718T>C	ENSP00000407473.2:p.Tyr240His
ENST00000473257.3:c.589T>C	ENSP00000501773.1:p.Tyr197His
ENST00000477812.2:n.1265T>C
ENST00000493945.6:c.718T>C	ENSP00000494269.1:p.Tyr240His
ENST00000642480.2:c.718T>C	ENSP00000495995.2:p.Tyr240His
ENST00000645576.1:c.670T>C	ENSP00000496101.1:p.Tyr224His
ENST00000646664.1:c.718T>C MANE Select	ENSP00000494750.1:p.Tyr240His
ENST00000647275.1:c.352T>C	ENSP00000494185.1:p.Tyr118His
ENST00000674681.1:c.718T>C	ENSP00000502821.1:p.Tyr240His
ENST00000675515.1:c.718T>C	ENSP00000501862.1:p.Tyr240His
ENST00000676189.1:c.*261T>C	ENSP00000502538.1:n.*261T>C
ENST00000676319.1:c.88-582T>C	ENSP00000502193.1:n.88-582T>C
ENST00000676397.1:c.718T>C	ENSP00000502286.1:p.Tyr240His
ENST00000331789.9:c.718T>C	ENSP00000349960.4:p.Tyr240His
ENST00000425660.5:c.*381T>C	ENSP00000409264.1:n.*381T>C
ENST00000462494.5:n.1243T>C
ENST00000473257.1:n.436T>C
ENST00000484841.5:n.873T>C
ENST00000493945.5:n.724T>C
NM_001101.3:c.718T>C , LRG_132t1:c.718T>C	NP_001092.1:p.Tyr240His
XM_006715764.1:c.352T>C	XP_006715827.1:p.Tyr118His
NM_001101.4:c.718T>C	NP_001092.1:p.Tyr240His
NM_001101.5:c.718T>C MANE Select	NP_001092.1:p.Tyr240His