Canonical Allele Identifier: CA2335155695

Gene: ACTN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38708211_38708212delinsTC , CM000681.2:g.38708211_38708212delinsTC	GRCh38
NC_000019.9:g.39198851_39198852delinsTC , CM000681.1:g.39198851_39198852delinsTC	GRCh37
NC_000019.8:g.43890691_43890692delinsTC	NCBI36
NG_007082.2:g.65525_65526delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440400.3:c.651+16_651+17delinsTC	ENSP00000398393.2:n.651+16_651+17delinsTC
ENST00000697712.1:c.510+16_510+17delinsTC	ENSP00000513410.1:n.510+16_510+17delinsTC
ENST00000252699.7:c.651+16_651+17delinsTC MANE Select	ENSP00000252699.2:n.651+16_651+17delinsTC
ENST00000424234.7:c.651+16_651+17delinsTC	ENSP00000411187.4:n.651+16_651+17delinsTC
ENST00000440400.2:c.651+16_651+17delinsTC	ENSP00000398393.2:n.651+16_651+17delinsTC
ENST00000252699.6:c.651+16_651+17delinsTC	ENSP00000252699.2:n.651+16_651+17delinsTC
ENST00000390009.7:c.163-6258_163-6257delinsTC	ENSP00000439497.1:n.163-6258_163-6257delinsTC
ENST00000424234.6:c.272+7502_272+7503delinsTC	ENSP00000411187.3:n.272+7502_272+7503delinsTC
ENST00000495553.1:n.557+16_557+17delinsTC
ENST00000586538.1:c.54+16_54+17delinsTC	ENSP00000465176.1:n.54+16_54+17delinsTC
ENST00000588618.5:n.748+16_748+17delinsTC
ENST00000589528.1:c.285+7497_285+7498delinsTC
NM_004924.4:c.651+16_651+17delinsTC	NP_004915.2:n.651+16_651+17delinsTC
XM_005259281.3:c.651+16_651+17delinsTC	XP_005259338.1:n.651+16_651+17delinsTC
XM_005259282.3:c.651+16_651+17delinsTC	XP_005259339.1:n.651+16_651+17delinsTC
XM_006723406.1:c.651+16_651+17delinsTC	XP_006723469.1:n.651+16_651+17delinsTC
NM_001322033.1:c.651+16_651+17delinsTC	NP_001308962.1:n.651+16_651+17delinsTC
NM_004924.5:c.651+16_651+17delinsTC	NP_004915.2:n.651+16_651+17delinsTC
XM_005259281.5:c.651+16_651+17delinsTC	XP_005259338.1:n.651+16_651+17delinsTC
XM_006723406.3:c.651+16_651+17delinsTC	XP_006723469.1:n.651+16_651+17delinsTC
XM_017027331.2:c.651+16_651+17delinsTC	XP_016882820.1:n.651+16_651+17delinsTC
XR_001753937.1:n.123-6048_123-6047delinsGA
NM_004924.6:c.651+16_651+17delinsTC MANE Select	NP_004915.2:n.651+16_651+17delinsTC
NM_001322033.2:c.651+16_651+17delinsTC	NP_001308962.1:n.651+16_651+17delinsTC