Canonical Allele Identifier: CA823942681

Gene: NOTCH4

Linked Data

• dbSNP Id: rs892532714
• MyVariant Identifiers: chr6:g.32170677_32170678insTATTAT (hg19) ; chr6:g.32202900_32202901insTATTAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32202914_32202919dup , CM000668.2:g.32202914_32202919dup	GRCh38
NC_000006.11:g.32170691_32170696dup , CM000668.1:g.32170691_32170696dup	GRCh37
NC_000006.10:g.32278669_32278674dup	NCBI36
NG_028190.1:g.26162_26167dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375023.3:c.3232-307_3232-302dup MANE Select	ENSP00000364163.3:n.3232-307_3232-302dup
ENST00000474612.1:n.1011_1016dup
NM_004557.3:c.3232-307_3232-302dup	NP_004548.3:n.3232-307_3232-302dup
NR_134949.1:n.3472+864_3472+869dup
NR_134950.1:n.3370+864_3370+869dup
NM_004557.4:c.3232-307_3232-302dup MANE Select	NP_004548.3:n.3232-307_3232-302dup
NR_134949.2:n.3472+864_3472+869dup
NR_134950.2:n.3370+864_3370+869dup