Canonical Allele Identifier: CA2458086321
Gene: SMARCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.129523374G= , CM000685.2:g.129523374G= GRCh38
NC_000023.10:g.128657351G= , CM000685.1:g.128657351G= GRCh37
NC_000023.9:g.128485032G= NCBI36
NG_012526.1:g.5110C=

Transcript Alleles

HGVS Amino-acid change
ENST00000371121.5:c.-4C= MANE Select ENSP00000360162.4:n.-4C=
ENST00000371121.4:c.-4C= ENSP00000360162.4:n.-4C=
ENST00000371122.8:c.-4C= ENSP00000360163.4:n.-4C=
ENST00000371123.5:c.-4C= ENSP00000360164.2:n.-4C=
ENST00000617310.4:n.91C=
NM_001282874.1:c.-4C= NP_001269803.1:n.-4C=
NM_001282875.1:c.-4C= NP_001269804.1:n.-4C=
NM_003069.4:c.-4C= NP_003060.2:n.-4C=
XM_005262461.1:c.-4C= XP_005262518.1:n.-4C=
XM_005262462.1:c.-4C= XP_005262519.1:n.-4C=
XM_006724782.1:c.-4C= XP_006724845.1:n.-4C=
XM_005262461.2:c.-4C= XP_005262518.1:n.-4C=
XM_005262462.2:c.-4C= XP_005262519.1:n.-4C=
XM_006724782.2:c.-4C= XP_006724845.1:n.-4C=
XM_017029750.1:c.-4C= XP_016885239.1:n.-4C=
XM_017029751.1:c.-4C= XP_016885240.1:n.-4C=
NM_001282874.2:c.-4C= MANE Select NP_001269803.1:n.-4C=
NM_001282875.2:c.-4C= NP_001269804.1:n.-4C=
NM_003069.5:c.-4C= NP_003060.2:n.-4C=
NM_001378261.1:c.-4C= NP_001365190.1:n.-4C=
NM_001378262.1:c.-4C= NP_001365191.1:n.-4C=
NM_001378263.1:c.-4C= NP_001365192.1:n.-4C=
NM_001378264.1:c.-4C= NP_001365193.1:n.-4C=