Canonical Allele Identifier: CA2216733601

Gene: SRCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30737371G= , CM000678.2:g.30737371G=	GRCh38
NC_000016.9:g.30748692G= , CM000678.1:g.30748692G=	GRCh37
NC_000016.8:g.30656193G=	NCBI36
NG_032135.1:g.43231G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411466.7:c.7331G=	ENSP00000405186.3:p.Arg2444=
ENST00000704023.1:c.1593+18G=
ENST00000706321.1:c.7331G=	ENSP00000516346.1:p.Arg2444=
ENST00000262518.9:c.7331G= MANE Select	ENSP00000262518.4:p.Arg2444=
ENST00000262518.8:c.7331G=	ENSP00000262518.4:p.Arg2444=
ENST00000380361.7:c.6800G=	ENSP00000369719.3:p.Arg2267=
ENST00000395059.6:c.6554G=	ENSP00000378499.3:p.Arg2185=
NM_006662.2:c.7331G=	NP_006653.2:p.Arg2444=
NM_006662.3:c.7331G= MANE Select	NP_006653.2:p.Arg2444=