Canonical Allele Identifier: CA375631191

Gene: NOTCH1

Linked Data

• dbSNP Id: rs1315402658
• MyVariant Identifiers: chr9:g.139391613C>A (hg19) ; chr9:g.136497161C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497161C>A , CM000671.2:g.136497161C>A	GRCh38
NC_000009.11:g.139391613C>A , CM000671.1:g.139391613C>A	GRCh37
NC_000009.10:g.138511434C>A	NCBI36
NG_007458.1:g.53626G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6578G>T MANE Select	ENSP00000498587.1:p.Ser2193Ile
ENST00000679595.1:c.*1618G>T	ENSP00000506241.1:n.*1618G>T
ENST00000679969.1:n.3174G>T
ENST00000680003.1:n.2910G>T
ENST00000680133.1:c.6464G>T	ENSP00000505319.1:p.Ser2155Ile
ENST00000680218.1:c.6458G>T	ENSP00000505339.1:p.Ser2153Ile
ENST00000680668.1:c.6464G>T	ENSP00000506336.1:p.Ser2155Ile
ENST00000680778.1:c.4175G>T	ENSP00000506033.1:p.Ser1392Ile
ENST00000680924.1:c.*3978G>T	ENSP00000506031.1:n.*3978G>T
ENST00000681135.1:c.*4187G>T	ENSP00000506636.1:n.*4187G>T
ENST00000681298.1:n.4683G>T
ENST00000681454.1:c.*5814G>T	ENSP00000505763.1:n.*5814G>T
ENST00000277541.6:c.6578G>T	ENSP00000277541.6:p.Ser2193Ile
NM_017617.3:c.6578G>T	NP_060087.3:p.Ser2193Ile
XM_011518717.1:c.5879G>T	XP_011517019.1:p.Ser1960Ile
NM_017617.5:c.6578G>T MANE Select	NP_060087.3:p.Ser2193Ile
XM_011518717.2:c.5855G>T	XP_011517019.2:p.Ser1952Ile