Canonical Allele Identifier: CA8012803
Community Standard Title: NM_006662.3(SRCAP):c.8963C>T (p.Thr2988Ile)
Gene: SRCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30739003C>T , CM000678.2:g.30739003C>T GRCh38
NC_000016.9:g.30750324C>T , CM000678.1:g.30750324C>T GRCh37
NC_000016.8:g.30657825C>T NCBI36
NG_032135.1:g.44863C>T

Transcript Alleles

HGVS Amino-acid Change
NM_006662.3:c.8963C>T MANE Select NP_006653.2:p.Thr2988Ile
ENST00000262518.9:c.8963C>T MANE Select ENSP00000262518.4:p.Thr2988Ile
NM_006662.2:c.8963C>T NP_006653.2:p.Thr2988Ile
ENST00000262518.8:c.8963C>T ENSP00000262518.4:p.Thr2988Ile
ENST00000380361.7:c.8432C>T ENSP00000369719.3:p.Thr2811Ile
ENST00000395059.6:c.8186C>T ENSP00000378499.3:p.Thr2729Ile
ENST00000411466.7:c.8963C>T ENSP00000405186.3:p.Thr2988Ile
ENST00000704023.1:c.1758+1048C>T
ENST00000706321.1:c.8963C>T ENSP00000516346.1:p.Thr2988Ile