Canonical Allele Identifier: CA494910530
Gene: SRCAP HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.30748612C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30737291C>T , CM000678.2:g.30737291C>T GRCh38
NC_000016.9:g.30748612C>T , CM000678.1:g.30748612C>T GRCh37
NC_000016.8:g.30656113C>T NCBI36
NG_032135.1:g.43151C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000411466.7:c.7251C>T ENSP00000405186.3:p.Ala2417=
ENST00000704023.1:c.1531C>T
ENST00000706321.1:c.7251C>T ENSP00000516346.1:p.Ala2417=
ENST00000262518.9:c.7251C>T MANE Select ENSP00000262518.4:p.Ala2417=
ENST00000262518.8:c.7251C>T ENSP00000262518.4:p.Ala2417=
ENST00000380361.7:c.6720C>T ENSP00000369719.3:p.Ala2240=
ENST00000395059.6:c.6474C>T ENSP00000378499.3:p.Ala2158=
NM_006662.2:c.7251C>T NP_006653.2:p.Ala2417=
NM_006662.3:c.7251C>T MANE Select NP_006653.2:p.Ala2417=