Canonical Allele Identifier: CA2575971362

Gene: SRCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30736522C>G , CM000678.2:g.30736522C>G	GRCh38
NC_000016.9:g.30747843C>G , CM000678.1:g.30747843C>G	GRCh37
NC_000016.8:g.30655344C>G	NCBI36
NG_032135.1:g.42382C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006662.3:c.6925-19C>G MANE Select	NP_006653.2:n.6925-19C>G
ENST00000262518.9:c.6925-19C>G MANE Select	ENSP00000262518.4:n.6925-19C>G
NM_006662.2:c.6925-19C>G	NP_006653.2:n.6925-19C>G
ENST00000262518.8:c.6925-19C>G	ENSP00000262518.4:n.6925-19C>G
ENST00000380361.7:c.6394-19C>G	ENSP00000369719.3:n.6394-19C>G
ENST00000395059.6:c.6148-19C>G	ENSP00000378499.3:n.6148-19C>G
ENST00000411466.7:c.6925-19C>G	ENSP00000405186.3:n.6925-19C>G
ENST00000704023.1:c.1205-19C>G
ENST00000706321.1:c.6925-19C>G	ENSP00000516346.1:n.6925-19C>G