Canonical Allele Identifier: CA10378023
Community Standard Title: NM_004006.3(DMD):c.8651T>C (p.Leu2884Pro)
Gene: DMD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.31479000A>G , CM000685.2:g.31479000A>G GRCh38
NC_000023.10:g.31497117A>G , CM000685.1:g.31497117A>G GRCh37
NC_000023.9:g.31407038A>G NCBI36
NG_012232.1:g.1865610T>C , LRG_199:g.1865610T>C

Transcript Alleles

HGVS Amino-acid Change
NM_004006.3:c.8651T>C MANE Select NP_003997.2:p.Leu2884Pro
ENST00000357033.9:c.8651T>C MANE Select ENSP00000354923.3:p.Leu2884Pro
NM_000109.3:c.8627T>C NP_000100.2:p.Leu2876Pro
NM_000109.4:c.8627T>C NP_000100.3:p.Leu2876Pro
NM_004006.2:c.8651T>C , LRG_199t1:c.8651T>C NP_003997.1:p.Leu2884Pro
NM_004009.3:c.8639T>C NP_004000.1:p.Leu2880Pro
NM_004010.3:c.8282T>C NP_004001.1:p.Leu2761Pro
NM_004011.3:c.4628T>C NP_004002.2:p.Leu1543Pro
NM_004011.4:c.4628T>C NP_004002.3:p.Leu1543Pro
NM_004012.3:c.4619T>C NP_004003.1:p.Leu1540Pro
NM_004012.4:c.4619T>C NP_004003.2:p.Leu1540Pro
NM_004013.2:c.1271T>C NP_004004.1:p.Leu424Pro
NM_004013.3:c.1271T>C NP_004004.2:p.Leu424Pro
NM_004014.2:c.464T>C NP_004005.1:p.Leu155Pro
NM_004014.3:c.464T>C NP_004005.2:p.Leu155Pro
NM_004020.3:c.1271T>C NP_004011.2:p.Leu424Pro
NM_004020.4:c.1271T>C NP_004011.3:p.Leu424Pro
NM_004021.2:c.1271T>C NP_004012.1:p.Leu424Pro
NM_004021.3:c.1271T>C NP_004012.2:p.Leu424Pro
NM_004022.2:c.1271T>C NP_004013.1:p.Leu424Pro
NM_004022.3:c.1271T>C NP_004013.2:p.Leu424Pro
NM_004023.2:c.1271T>C NP_004014.1:p.Leu424Pro
NM_004023.3:c.1271T>C NP_004014.2:p.Leu424Pro
ENST00000343523.6:c.464T>C ENSP00000340057.3:p.Leu155Pro
ENST00000343523.7:c.506T>C ENSP00000340057.4:p.Leu169Pro
ENST00000357033.8:c.8651T>C ENSP00000354923.3:p.Leu2884Pro
ENST00000358062.6:c.1739T>C ENSP00000350765.2:p.Leu580Pro
ENST00000358062.7:c.3497T>C ENSP00000350765.3:p.Leu1166Pro
ENST00000359836.5:c.1271T>C ENSP00000352894.1:p.Leu424Pro
ENST00000378677.6:c.8639T>C ENSP00000367948.2:p.Leu2880Pro
ENST00000378707.7:c.1271T>C ENSP00000367979.3:p.Leu424Pro
ENST00000445312.1:n.708T>C
ENST00000474231.5:c.1271T>C ENSP00000417123.1:p.Leu424Pro
ENST00000541735.5:c.1271T>C ENSP00000444119.1:p.Leu424Pro
ENST00000619831.4:c.8636T>C ENSP00000479270.1:p.Leu2879Pro
ENST00000619831.5:c.4619T>C ENSP00000479270.2:p.Leu1540Pro
ENST00000620040.4:c.8648T>C ENSP00000478150.1:p.Leu2883Pro
ENST00000620040.5:c.1271T>C ENSP00000478150.2:p.Leu424Pro
ENST00000680961.1:c.1271T>C ENSP00000506386.1:p.Leu424Pro
ENST00000681646.1:n.2312T>C
ENST00000682238.1:c.1271T>C ENSP00000508124.1:p.Leu424Pro
ENST00000683450.1:n.2116T>C
ENST00000683957.1:n.2143T>C
ENST00000684130.1:c.1271T>C ENSP00000508037.1:p.Leu424Pro
XM_006724468.2:c.8651T>C XP_006724531.1:p.Leu2884Pro
XM_006724469.2:c.8627T>C XP_006724532.1:p.Leu2876Pro
XM_006724469.3:c.8627T>C XP_006724532.1:p.Leu2876Pro
XM_006724470.2:c.8651T>C XP_006724533.1:p.Leu2884Pro
XM_006724470.3:c.8651T>C XP_006724533.1:p.Leu2884Pro
XM_006724471.2:c.8651T>C XP_006724534.1:p.Leu2884Pro
XM_006724472.2:c.8522T>C XP_006724535.1:p.Leu2841Pro
XM_006724473.2:c.8513T>C XP_006724536.1:p.Leu2838Pro
XM_006724474.2:c.8651T>C XP_006724537.1:p.Leu2884Pro
XM_006724474.3:c.8651T>C XP_006724537.1:p.Leu2884Pro
XM_006724475.2:c.8651T>C XP_006724538.1:p.Leu2884Pro
XM_011545467.1:c.8528T>C XP_011543769.1:p.Leu2843Pro
XM_011545468.1:c.8651T>C XP_011543770.1:p.Leu2884Pro
XM_011545468.2:c.8651T>C XP_011543770.1:p.Leu2884Pro
XM_017029328.1:c.8651T>C XP_016884817.1:p.Leu2884Pro
XM_017029331.1:c.2825T>C XP_016884820.1:p.Leu942Pro