Canonical Allele Identifier: CA375631205

Gene: NOTCH1

Linked Data

• MyVariant Identifiers: chr9:g.139391616T>G (hg19) ; chr9:g.136497164T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136497164T>G , CM000671.2:g.136497164T>G	GRCh38
NC_000009.11:g.139391616T>G , CM000671.1:g.139391616T>G	GRCh37
NC_000009.10:g.138511437T>G	NCBI36
NG_007458.1:g.53623A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651671.1:c.6575A>C MANE Select	ENSP00000498587.1:p.Asp2192Ala
ENST00000679595.1:c.*1615A>C	ENSP00000506241.1:n.*1615A>C
ENST00000679969.1:n.3171A>C
ENST00000680003.1:n.2907A>C
ENST00000680133.1:c.6461A>C	ENSP00000505319.1:p.Asp2154Ala
ENST00000680218.1:c.6455A>C	ENSP00000505339.1:p.Asp2152Ala
ENST00000680668.1:c.6461A>C	ENSP00000506336.1:p.Asp2154Ala
ENST00000680778.1:c.4172A>C	ENSP00000506033.1:p.Asp1391Ala
ENST00000680924.1:c.*3975A>C	ENSP00000506031.1:n.*3975A>C
ENST00000681135.1:c.*4184A>C	ENSP00000506636.1:n.*4184A>C
ENST00000681298.1:n.4680A>C
ENST00000681454.1:c.*5811A>C	ENSP00000505763.1:n.*5811A>C
ENST00000277541.6:c.6575A>C	ENSP00000277541.6:p.Asp2192Ala
NM_017617.3:c.6575A>C	NP_060087.3:p.Asp2192Ala
XM_011518717.1:c.5876A>C	XP_011517019.1:p.Asp1959Ala
NM_017617.5:c.6575A>C MANE Select	NP_060087.3:p.Asp2192Ala
XM_011518717.2:c.5852A>C	XP_011517019.2:p.Asp1951Ala