Canonical Allele Identifier: CA354805798

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188979T>C (hg19) ; chr3:g.142470137T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470137T>C , CM000665.2:g.142470137T>C	GRCh38
NC_000003.11:g.142188979T>C , CM000665.1:g.142188979T>C	GRCh37
NC_000003.10:g.143671669T>C	NCBI36
NG_008951.1:g.113690A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6268A>G MANE Select	ENSP00000343741.4:p.Met2090Val
ENST00000513291.2:n.1452A>G
ENST00000654170.1:n.1111A>G
ENST00000656590.1:c.5058A>G
ENST00000661310.1:c.6076A>G	ENSP00000499589.1:p.Met2026Val
ENST00000665483.1:n.123A>G
ENST00000666447.1:n.103A>G
ENST00000666943.1:n.1732A>G
ENST00000350721.8:c.6268A>G	ENSP00000343741.4:p.Met2090Val
NM_001184.3:c.6268A>G	NP_001175.2:p.Met2090Val
XM_011512924.1:c.6274A>G	XP_011511226.1:p.Met2092Val
XM_011512925.1:c.6082A>G	XP_011511227.1:p.Met2028Val
XR_924147.1:n.6363A>G
XR_924148.1:n.6363A>G
XR_924149.1:n.6242A>G
NM_001354579.1:c.6076A>G	NP_001341508.1:p.Met2026Val
XR_001740179.2:n.6357A>G
XR_001740180.2:n.6411A>G
XR_001740181.2:n.6290A>G
XR_001740182.1:n.6242A>G
XR_002959543.1:n.6467A>G
XR_924148.2:n.6363A>G
NM_001184.4:c.6268A>G MANE Select	NP_001175.2:p.Met2090Val
NM_001354579.2:c.6076A>G	NP_001341508.1:p.Met2026Val