Canonical Allele Identifier: CA2537260301

Gene: ACTB

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5529368_5529369insCT , CM000669.2:g.5529368_5529369insCT	GRCh38
NC_000007.13:g.5568999_5569000insCT , CM000669.1:g.5568999_5569000insCT	GRCh37
NC_000007.12:g.5535525_5535526insCT	NCBI36
NG_007992.1:g.6233_6234insAG , LRG_132:g.6233_6234insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000417101.2:c.155_156insAG	ENSP00000399487.2:p.Tyr53AlafsTer16
ENST00000432588.6:c.155_156insAG	ENSP00000407473.2:p.Tyr53AlafsTer16
ENST00000473257.3:c.26_27insAG	ENSP00000501773.1:p.Tyr10AlafsTer16
ENST00000477812.2:n.362_363insAG
ENST00000484841.6:n.309_310insAG
ENST00000493945.6:c.155_156insAG	ENSP00000494269.1:p.Tyr53AlafsTer16
ENST00000642480.2:c.155_156insAG	ENSP00000495995.2:p.Tyr53AlafsTer16
ENST00000645025.1:n.238_239insAG
ENST00000645576.1:c.155_156insAG	ENSP00000496101.1:p.Tyr53AlafsTer16
ENST00000646664.1:c.155_156insAG MANE Select	ENSP00000494750.1:p.Tyr53AlafsTer16
ENST00000647275.1:c.-3-650_-3-649insAG	ENSP00000494185.1:n.-3-650_-3-649insAG
ENST00000674681.1:c.155_156insAG	ENSP00000502821.1:p.Tyr53AlafsTer16
ENST00000675515.1:c.155_156insAG	ENSP00000501862.1:p.Tyr53AlafsTer16
ENST00000676189.1:c.155_156insAG	ENSP00000502538.1:p.Tyr53AlafsTer16
ENST00000676319.1:c.87+202_87+203insAG	ENSP00000502193.1:n.87+202_87+203insAG
ENST00000676397.1:c.155_156insAG	ENSP00000502286.1:p.Tyr53AlafsTer16
ENST00000331789.9:c.155_156insAG	ENSP00000349960.4:p.Tyr53AlafsTer16
ENST00000414620.1:c.155_156insAG	ENSP00000401032.1:p.Tyr53AlafsTer16
ENST00000417101.1:c.164_165insAG	ENSP00000399487.1:p.Tyr56AlafsTer16
ENST00000425660.5:c.155_156insAG	ENSP00000409264.1:p.Tyr53AlafsTer16
ENST00000432588.5:c.155_156insAG	ENSP00000407473.1:p.Tyr53AlafsTer16
ENST00000443528.5:c.155_156insAG	ENSP00000393951.1:p.Tyr53AlafsTer16
ENST00000462494.5:n.239_240insAG
ENST00000473257.1:n.82-650_82-649insAG
ENST00000477812.1:n.362_363insAG
ENST00000480301.1:n.355_356insAG
ENST00000484841.5:n.310_311insAG
ENST00000493945.5:n.161_162insAG
NM_001101.3:c.155_156insAG , LRG_132t1:c.155_156insAG	NP_001092.1:p.Tyr53AlafsTer16
NM_001101.4:c.155_156insAG	NP_001092.1:p.Tyr53AlafsTer16
NM_001101.5:c.155_156insAG MANE Select	NP_001092.1:p.Tyr53AlafsTer16