Canonical Allele Identifier: CA354806159

Gene: ATR

Linked Data

• gnomAD v4: 3-142470185-T-C
• MyVariant Identifiers: chr3:g.142189027T>C (hg19) ; chr3:g.142470185T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470185T>C , CM000665.2:g.142470185T>C	GRCh38
NC_000003.11:g.142189027T>C , CM000665.1:g.142189027T>C	GRCh37
NC_000003.10:g.143671717T>C	NCBI36
NG_008951.1:g.113642A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6222-2A>G MANE Select	ENSP00000343741.4:n.6222-2A>G
ENST00000513291.2:n.1406-2A>G
ENST00000654170.1:n.1065-2A>G
ENST00000656590.1:c.5012-2A>G
ENST00000661310.1:c.6030-2A>G	ENSP00000499589.1:n.6030-2A>G
ENST00000665483.1:n.77-2A>G
ENST00000666447.1:n.57-2A>G
ENST00000666943.1:n.1686-2A>G
ENST00000350721.8:c.6222-2A>G	ENSP00000343741.4:n.6222-2A>G
NM_001184.3:c.6222-2A>G	NP_001175.2:n.6222-2A>G
XM_011512924.1:c.6228-2A>G	XP_011511226.1:n.6228-2A>G
XM_011512925.1:c.6036-2A>G	XP_011511227.1:n.6036-2A>G
XR_924147.1:n.6317-2A>G
XR_924148.1:n.6317-2A>G
XR_924149.1:n.6196-2A>G
NM_001354579.1:c.6030-2A>G	NP_001341508.1:n.6030-2A>G
XR_001740179.2:n.6311-2A>G
XR_001740180.2:n.6365-2A>G
XR_001740181.2:n.6244-2A>G
XR_001740182.1:n.6196-2A>G
XR_002959543.1:n.6421-2A>G
XR_924148.2:n.6317-2A>G
NM_001184.4:c.6222-2A>G MANE Select	NP_001175.2:n.6222-2A>G
NM_001354579.2:c.6030-2A>G	NP_001341508.1:n.6030-2A>G