Canonical Allele Identifier: CA412668800
Community Standard Title: NM_004006.3(DMD):c.822T>A (p.Tyr274Ter)
Gene: DMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.32699121A>T , CM000685.2:g.32699121A>T GRCh38
NC_000023.10:g.32717238A>T , CM000685.1:g.32717238A>T GRCh37
NC_000023.9:g.32627159A>T NCBI36
NG_012232.1:g.645489T>A , LRG_199:g.645489T>A

Transcript Alleles

HGVS Amino-acid Change
NM_004006.3:c.822T>A MANE Select NP_003997.2:p.Tyr274Ter
ENST00000357033.9:c.822T>A MANE Select ENSP00000354923.3:p.Tyr274Ter
NM_000109.3:c.798T>A NP_000100.2:p.Tyr266Ter
NM_000109.4:c.798T>A NP_000100.3:p.Tyr266Ter
NM_004006.2:c.822T>A , LRG_199t1:c.822T>A NP_003997.1:p.Tyr274Ter
NM_004009.3:c.810T>A NP_004000.1:p.Tyr270Ter
NM_004010.3:c.453T>A NP_004001.1:p.Tyr151Ter
ENST00000288447.8:c.798T>A ENSP00000288447.4:p.Tyr266Ter
ENST00000288447.9:c.798T>A ENSP00000288447.4:p.Tyr266Ter
ENST00000357033.8:c.822T>A ENSP00000354923.3:p.Tyr274Ter
ENST00000378677.6:c.810T>A ENSP00000367948.2:p.Tyr270Ter
ENST00000420596.5:c.93+321018T>A ENSP00000399897.1:n.93+321018T>A
ENST00000447523.1:c.246+124174T>A ENSP00000395904.1:n.246+124174T>A
ENST00000448370.5:c.93+321018T>A ENSP00000388559.1:n.93+321018T>A
ENST00000480751.1:n.86+117347T>A
ENST00000488902.5:n.335+321018T>A
ENST00000619831.4:c.810T>A ENSP00000479270.1:p.Tyr270Ter
ENST00000620040.4:c.822T>A ENSP00000478150.1:p.Tyr274Ter
ENST00000682071.1:c.453T>A ENSP00000508133.1:p.Tyr151Ter
ENST00000682870.1:n.1007T>A
ENST00000682899.1:n.1029T>A
ENST00000682924.1:c.822T>A ENSP00000508187.1:p.Tyr274Ter
ENST00000683985.1:n.1029T>A
ENST00000684165.1:n.1029T>A
ENST00000684237.1:c.822T>A ENSP00000507277.1:p.Tyr274Ter
ENST00000684292.1:n.1029T>A
ENST00000684660.1:n.1007T>A
XM_006724468.2:c.822T>A XP_006724531.1:p.Tyr274Ter
XM_006724469.2:c.798T>A XP_006724532.1:p.Tyr266Ter
XM_006724469.3:c.798T>A XP_006724532.1:p.Tyr266Ter
XM_006724470.2:c.822T>A XP_006724533.1:p.Tyr274Ter
XM_006724470.3:c.822T>A XP_006724533.1:p.Tyr274Ter
XM_006724471.2:c.822T>A XP_006724534.1:p.Tyr274Ter
XM_006724472.2:c.822T>A XP_006724535.1:p.Tyr274Ter
XM_006724473.2:c.822T>A XP_006724536.1:p.Tyr274Ter
XM_006724474.2:c.822T>A XP_006724537.1:p.Tyr274Ter
XM_006724474.3:c.822T>A XP_006724537.1:p.Tyr274Ter
XM_006724475.2:c.822T>A XP_006724538.1:p.Tyr274Ter
XM_011545467.1:c.822T>A XP_011543769.1:p.Tyr274Ter
XM_011545468.1:c.822T>A XP_011543770.1:p.Tyr274Ter
XM_011545468.2:c.822T>A XP_011543770.1:p.Tyr274Ter
XM_011545469.1:c.822T>A XP_011543771.1:p.Tyr274Ter
XM_017029328.1:c.822T>A XP_016884817.1:p.Tyr274Ter
XM_017029329.1:c.822T>A XP_016884818.1:p.Tyr274Ter
XM_017029330.2:c.822T>A XP_016884819.1:p.Tyr274Ter