Canonical Allele Identifier: CA8012473
Community Standard Title: NM_006662.3(SRCAP):c.7378G>A (p.Val2460Ile)
Gene: SRCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30737418G>A , CM000678.2:g.30737418G>A GRCh38
NC_000016.9:g.30748739G>A , CM000678.1:g.30748739G>A GRCh37
NC_000016.8:g.30656240G>A NCBI36
NG_032135.1:g.43278G>A

Transcript Alleles

HGVS Amino-acid Change
NM_006662.3:c.7378G>A MANE Select NP_006653.2:p.Val2460Ile
ENST00000262518.9:c.7378G>A MANE Select ENSP00000262518.4:p.Val2460Ile
NM_006662.2:c.7378G>A NP_006653.2:p.Val2460Ile
ENST00000262518.8:c.7378G>A ENSP00000262518.4:p.Val2460Ile
ENST00000380361.7:c.6847G>A ENSP00000369719.3:p.Val2283Ile
ENST00000395059.6:c.6601G>A ENSP00000378499.3:p.Val2201Ile
ENST00000411466.7:c.7378G>A ENSP00000405186.3:p.Val2460Ile
ENST00000704023.1:c.1593+65G>A
ENST00000706321.1:c.7378G>A ENSP00000516346.1:p.Val2460Ile