Canonical Allele Identifier: CA84751362

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142485514G>A , CM000665.2:g.142485514G>A	GRCh38
NC_000003.11:g.142204356G>A , CM000665.1:g.142204356G>A	GRCh37
NC_000003.10:g.143687046G>A	NCBI36
NG_008951.1:g.98313C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001184.4:c.6079-232C>T MANE Select	NP_001175.2:n.6079-232C>T
ENST00000350721.9:c.6079-232C>T MANE Select	ENSP00000343741.4:n.6079-232C>T
NM_001184.3:c.6079-232C>T	NP_001175.2:n.6079-232C>T
NM_001354579.1:c.5887-232C>T	NP_001341508.1:n.5887-232C>T
NM_001354579.2:c.5887-232C>T	NP_001341508.1:n.5887-232C>T
ENST00000350721.8:c.6079-232C>T	ENSP00000343741.4:n.6079-232C>T
ENST00000513291.2:n.1263-232C>T
ENST00000654170.1:n.690C>T
ENST00000656590.1:c.4869-232C>T
ENST00000661310.1:c.5887-232C>T	ENSP00000499589.1:n.5887-232C>T
ENST00000666943.1:n.1543-232C>T
XM_011512924.1:c.6085-232C>T	XP_011511226.1:n.6085-232C>T
XM_011512925.1:c.5893-232C>T	XP_011511227.1:n.5893-232C>T
XM_011512926.1:c.6085-232C>T	XP_011511228.1:n.6085-232C>T
XM_011512927.1:c.6085-184C>T	XP_011511229.1:n.6085-184C>T
XR_001740179.2:n.6168-232C>T
XR_001740180.2:n.6174-184C>T
XR_001740181.2:n.6053-184C>T
XR_001740182.1:n.6053-232C>T
XR_002959543.1:n.6174-232C>T
XR_924147.1:n.6174-232C>T
XR_924148.1:n.6174-232C>T
XR_924148.2:n.6174-232C>T
XR_924149.1:n.6053-232C>T