Canonical Allele Identifier: CA8012442
Gene: SRCAP HGNC NCBI

Linked Data

dbSNP Id: rs768912555

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30737278C>T , CM000678.2:g.30737278C>T GRCh38
NC_000016.9:g.30748599C>T , CM000678.1:g.30748599C>T GRCh37
NC_000016.8:g.30656100C>T NCBI36
NG_032135.1:g.43138C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000411466.7:c.7238C>T ENSP00000405186.3:p.Pro2413Leu
ENST00000704023.1:c.1518C>T
ENST00000706321.1:c.7238C>T ENSP00000516346.1:p.Pro2413Leu
ENST00000262518.9:c.7238C>T MANE Select ENSP00000262518.4:p.Pro2413Leu
ENST00000262518.8:c.7238C>T ENSP00000262518.4:p.Pro2413Leu
ENST00000380361.7:c.6707C>T ENSP00000369719.3:p.Pro2236Leu
ENST00000395059.6:c.6461C>T ENSP00000378499.3:p.Pro2154Leu
NM_006662.2:c.7238C>T NP_006653.2:p.Pro2413Leu
NM_006662.3:c.7238C>T MANE Select NP_006653.2:p.Pro2413Leu