Canonical Allele Identifier: CA993904770
Gene: NOTCH3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15187473_15187475dup , CM000681.2:g.15187473_15187475dup GRCh38
NC_000019.9:g.15298284_15298286dup , CM000681.1:g.15298284_15298286dup GRCh37
NC_000019.8:g.15159284_15159286dup NCBI36
NG_009819.1:g.18508_18510dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1607-136_1607-134dup MANE Select ENSP00000263388.1:n.1607-136_1607-134dup
ENST00000263388.6:c.1607-136_1607-134dup ENSP00000263388.1:n.1607-136_1607-134dup
ENST00000601011.1:c.1604-136_1604-134dup ENSP00000473138.1:n.1604-136_1604-134dup
NM_000435.2:c.1607-136_1607-134dup NP_000426.2:n.1607-136_1607-134dup
XM_005259924.3:c.1607-136_1607-134dup XP_005259981.1:n.1607-136_1607-134dup
XM_005259924.4:c.1607-136_1607-134dup XP_005259981.1:n.1607-136_1607-134dup
NM_000435.3:c.1607-136_1607-134dup MANE Select NP_000426.2:n.1607-136_1607-134dup