Canonical Allele Identifier: CA2216733040

Gene: SRCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30737172A= , CM000678.2:g.30737172A=	GRCh38
NC_000016.9:g.30748493A= , CM000678.1:g.30748493A=	GRCh37
NC_000016.8:g.30655994A=	NCBI36
NG_032135.1:g.43032A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411466.7:c.7132A=	ENSP00000405186.3:p.Thr2378=
ENST00000704023.1:c.1412A=
ENST00000706321.1:c.7132A=	ENSP00000516346.1:p.Thr2378=
ENST00000262518.9:c.7132A= MANE Select	ENSP00000262518.4:p.Thr2378=
ENST00000262518.8:c.7132A=	ENSP00000262518.4:p.Thr2378=
ENST00000380361.7:c.6601A=	ENSP00000369719.3:p.Thr2201=
ENST00000395059.6:c.6355A=	ENSP00000378499.3:p.Thr2119=
NM_006662.2:c.7132A=	NP_006653.2:p.Thr2378=
NM_006662.3:c.7132A= MANE Select	NP_006653.2:p.Thr2378=