Canonical Allele Identifier: CA2324747839
Gene: NOTCH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15187489_15187493delinsCACTT , CM000681.2:g.15187489_15187493delinsCACTT GRCh38
NC_000019.9:g.15298300_15298304delinsCACTT , CM000681.1:g.15298300_15298304delinsCACTT GRCh37
NC_000019.8:g.15159300_15159304delinsCACTT NCBI36
NG_009819.1:g.18489_18493delinsAAGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000263388.7:c.1607-155_1607-151delinsAAGTG MANE Select ENSP00000263388.1:n.1607-155_1607-151delinsAAGTG
ENST00000263388.6:c.1607-155_1607-151delinsAAGTG ENSP00000263388.1:n.1607-155_1607-151delinsAAGTG
ENST00000601011.1:c.1604-155_1604-151delinsAAGTG ENSP00000473138.1:n.1604-155_1604-151delinsAAGTG
NM_000435.2:c.1607-155_1607-151delinsAAGTG NP_000426.2:n.1607-155_1607-151delinsAAGTG
XM_005259924.3:c.1607-155_1607-151delinsAAGTG XP_005259981.1:n.1607-155_1607-151delinsAAGTG
XM_005259924.4:c.1607-155_1607-151delinsAAGTG XP_005259981.1:n.1607-155_1607-151delinsAAGTG
NM_000435.3:c.1607-155_1607-151delinsAAGTG MANE Select NP_000426.2:n.1607-155_1607-151delinsAAGTG