Canonical Allele Identifier: CA354805556

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188943A>C (hg19) ; chr3:g.142470101A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470101A>C , CM000665.2:g.142470101A>C	GRCh38
NC_000003.11:g.142188943A>C , CM000665.1:g.142188943A>C	GRCh37
NC_000003.10:g.143671633A>C	NCBI36
NG_008951.1:g.113726T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6304T>G MANE Select	ENSP00000343741.4:p.Tyr2102Asp
ENST00000513291.2:n.1488T>G
ENST00000654170.1:n.1147T>G
ENST00000656590.1:c.5094T>G
ENST00000661310.1:c.6112T>G	ENSP00000499589.1:p.Tyr2038Asp
ENST00000665483.1:n.159T>G
ENST00000666447.1:n.139T>G
ENST00000666943.1:n.1768T>G
ENST00000350721.8:c.6304T>G	ENSP00000343741.4:p.Tyr2102Asp
NM_001184.3:c.6304T>G	NP_001175.2:p.Tyr2102Asp
XM_011512924.1:c.6310T>G	XP_011511226.1:p.Tyr2104Asp
XM_011512925.1:c.6118T>G	XP_011511227.1:p.Tyr2040Asp
XR_924147.1:n.6399T>G
XR_924148.1:n.6399T>G
XR_924149.1:n.6278T>G
NM_001354579.1:c.6112T>G	NP_001341508.1:p.Tyr2038Asp
XR_001740179.2:n.6393T>G
XR_001740180.2:n.6447T>G
XR_001740181.2:n.6326T>G
XR_001740182.1:n.6278T>G
XR_002959543.1:n.6503T>G
XR_924148.2:n.6399T>G
NM_001184.4:c.6304T>G MANE Select	NP_001175.2:p.Tyr2102Asp
NM_001354579.2:c.6112T>G	NP_001341508.1:p.Tyr2038Asp