Canonical Allele Identifier: CA354805779

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188977C>G (hg19) ; chr3:g.142470135C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470135C>G , CM000665.2:g.142470135C>G	GRCh38
NC_000003.11:g.142188977C>G , CM000665.1:g.142188977C>G	GRCh37
NC_000003.10:g.143671667C>G	NCBI36
NG_008951.1:g.113692G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6270G>C MANE Select	ENSP00000343741.4:p.Met2090Ile
ENST00000513291.2:n.1454G>C
ENST00000654170.1:n.1113G>C
ENST00000656590.1:c.5060G>C
ENST00000661310.1:c.6078G>C	ENSP00000499589.1:p.Met2026Ile
ENST00000665483.1:n.125G>C
ENST00000666447.1:n.105G>C
ENST00000666943.1:n.1734G>C
ENST00000350721.8:c.6270G>C	ENSP00000343741.4:p.Met2090Ile
NM_001184.3:c.6270G>C	NP_001175.2:p.Met2090Ile
XM_011512924.1:c.6276G>C	XP_011511226.1:p.Met2092Ile
XM_011512925.1:c.6084G>C	XP_011511227.1:p.Met2028Ile
XR_924147.1:n.6365G>C
XR_924148.1:n.6365G>C
XR_924149.1:n.6244G>C
NM_001354579.1:c.6078G>C	NP_001341508.1:p.Met2026Ile
XR_001740179.2:n.6359G>C
XR_001740180.2:n.6413G>C
XR_001740181.2:n.6292G>C
XR_001740182.1:n.6244G>C
XR_002959543.1:n.6469G>C
XR_924148.2:n.6365G>C
NM_001184.4:c.6270G>C MANE Select	NP_001175.2:p.Met2090Ile
NM_001354579.2:c.6078G>C	NP_001341508.1:p.Met2026Ile