Canonical Allele Identifier: CA346888
Community Standard Title: NM_004006.3(DMD):c.572C>G (p.Ser191Ter)
Gene: DMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.32809570G>C , CM000685.2:g.32809570G>C GRCh38
NC_000023.10:g.32827687G>C , CM000685.1:g.32827687G>C GRCh37
NC_000023.9:g.32737608G>C NCBI36
NG_012232.1:g.535040C>G , LRG_199:g.535040C>G

Transcript Alleles

HGVS Amino-acid Change
NM_004006.3:c.572C>G MANE Select NP_003997.2:p.Ser191Ter
ENST00000357033.9:c.572C>G MANE Select ENSP00000354923.3:p.Ser191Ter
NM_000109.3:c.548C>G NP_000100.2:p.Ser183Ter
NM_000109.4:c.548C>G NP_000100.3:p.Ser183Ter
NM_004006.2:c.572C>G , LRG_199t1:c.572C>G NP_003997.1:p.Ser191Ter
NM_004009.3:c.560C>G NP_004000.1:p.Ser187Ter
NM_004010.3:c.203C>G NP_004001.1:p.Ser68Ter
ENST00000288447.8:c.548C>G ENSP00000288447.4:p.Ser183Ter
ENST00000288447.9:c.548C>G ENSP00000288447.4:p.Ser183Ter
ENST00000357033.8:c.572C>G ENSP00000354923.3:p.Ser191Ter
ENST00000378677.6:c.560C>G ENSP00000367948.2:p.Ser187Ter
ENST00000420596.5:c.93+210569C>G ENSP00000399897.1:n.93+210569C>G
ENST00000447523.1:c.246+13725C>G ENSP00000395904.1:n.246+13725C>G
ENST00000448370.5:c.93+210569C>G ENSP00000388559.1:n.93+210569C>G
ENST00000480751.1:n.86+6898C>G
ENST00000488902.5:n.335+210569C>G
ENST00000619831.4:c.560C>G ENSP00000479270.1:p.Ser187Ter
ENST00000620040.4:c.572C>G ENSP00000478150.1:p.Ser191Ter
ENST00000682071.1:c.203C>G ENSP00000508133.1:p.Ser68Ter
ENST00000682437.1:n.896C>G
ENST00000682870.1:n.757C>G
ENST00000682899.1:n.779C>G
ENST00000682924.1:c.572C>G ENSP00000508187.1:p.Ser191Ter
ENST00000683309.1:n.756C>G
ENST00000683658.1:n.917C>G
ENST00000683985.1:n.779C>G
ENST00000684056.1:n.756C>G
ENST00000684165.1:n.779C>G
ENST00000684237.1:c.572C>G ENSP00000507277.1:p.Ser191Ter
ENST00000684292.1:n.779C>G
ENST00000684660.1:n.757C>G
XM_006724468.2:c.572C>G XP_006724531.1:p.Ser191Ter
XM_006724469.2:c.548C>G XP_006724532.1:p.Ser183Ter
XM_006724469.3:c.548C>G XP_006724532.1:p.Ser183Ter
XM_006724470.2:c.572C>G XP_006724533.1:p.Ser191Ter
XM_006724470.3:c.572C>G XP_006724533.1:p.Ser191Ter
XM_006724471.2:c.572C>G XP_006724534.1:p.Ser191Ter
XM_006724472.2:c.572C>G XP_006724535.1:p.Ser191Ter
XM_006724473.2:c.572C>G XP_006724536.1:p.Ser191Ter
XM_006724474.2:c.572C>G XP_006724537.1:p.Ser191Ter
XM_006724474.3:c.572C>G XP_006724537.1:p.Ser191Ter
XM_006724475.2:c.572C>G XP_006724538.1:p.Ser191Ter
XM_011545467.1:c.572C>G XP_011543769.1:p.Ser191Ter
XM_011545468.1:c.572C>G XP_011543770.1:p.Ser191Ter
XM_011545468.2:c.572C>G XP_011543770.1:p.Ser191Ter
XM_011545469.1:c.572C>G XP_011543771.1:p.Ser191Ter
XM_017029328.1:c.572C>G XP_016884817.1:p.Ser191Ter
XM_017029329.1:c.572C>G XP_016884818.1:p.Ser191Ter
XM_017029330.2:c.572C>G XP_016884819.1:p.Ser191Ter