Canonical Allele Identifier: CA2216733372
Gene: SRCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30737297A= , CM000678.2:g.30737297A= GRCh38
NC_000016.9:g.30748618A= , CM000678.1:g.30748618A= GRCh37
NC_000016.8:g.30656119A= NCBI36
NG_032135.1:g.43157A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000411466.7:c.7257A= ENSP00000405186.3:p.Gln2419=
ENST00000704023.1:c.1537A=
ENST00000706321.1:c.7257A= ENSP00000516346.1:p.Gln2419=
ENST00000262518.9:c.7257A= MANE Select ENSP00000262518.4:p.Gln2419=
ENST00000262518.8:c.7257A= ENSP00000262518.4:p.Gln2419=
ENST00000380361.7:c.6726A= ENSP00000369719.3:p.Gln2242=
ENST00000395059.6:c.6480A= ENSP00000378499.3:p.Gln2160=
NM_006662.2:c.7257A= NP_006653.2:p.Gln2419=
NM_006662.3:c.7257A= MANE Select NP_006653.2:p.Gln2419=