Canonical Allele Identifier: CA2649441

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142493223A>G , CM000665.2:g.142493223A>G	GRCh38
NC_000003.11:g.142212065A>G , CM000665.1:g.142212065A>G	GRCh37
NC_000003.10:g.143694755A>G	NCBI36
NG_008951.1:g.90604T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.5987T>C MANE Select	ENSP00000343741.4:p.Met1996Thr
ENST00000513291.2:n.1171T>C
ENST00000653868.1:n.6016T>C
ENST00000656590.1:c.4777T>C
ENST00000661310.1:c.5795T>C	ENSP00000499589.1:p.Met1932Thr
ENST00000666943.1:n.1451T>C
ENST00000350721.8:c.5987T>C	ENSP00000343741.4:p.Met1996Thr
NM_001184.3:c.5987T>C	NP_001175.2:p.Met1996Thr
XM_011512924.1:c.5993T>C	XP_011511226.1:p.Met1998Thr
XM_011512925.1:c.5801T>C	XP_011511227.1:p.Met1934Thr
XM_011512926.1:c.5993T>C	XP_011511228.1:p.Met1998Thr
XM_011512927.1:c.5993T>C	XP_011511229.1:p.Met1998Thr
XR_924147.1:n.6082T>C
XR_924148.1:n.6082T>C
XR_924149.1:n.5961T>C
NM_001354579.1:c.5795T>C	NP_001341508.1:p.Met1932Thr
XR_001740179.2:n.6076T>C
XR_001740180.2:n.6082T>C
XR_001740181.2:n.5961T>C
XR_001740182.1:n.5961T>C
XR_002959543.1:n.6082T>C
XR_924148.2:n.6082T>C
NM_001184.4:c.5987T>C MANE Select	NP_001175.2:p.Met1996Thr
NM_001354579.2:c.5795T>C	NP_001341508.1:p.Met1932Thr