Canonical Allele Identifier: CA10378822

Gene: DMD

Linked Data

• ClinVar Variation Id: 2016212
• ClinVar RCV Id: RCV002851459
• dbSNP Id: rs373723470
• ExAC: X:32383234 C / G
• gnomAD v2: X-32383234-C-G
• gnomAD v3: X-32365117-C-G
• gnomAD v4: X-32365117-C-G
• MyVariant Identifiers: chrX:g.32383234C>G (hg19) ; chrX:g.32365117C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32365117C>G , CM000685.2:g.32365117C>G	GRCh38
NC_000023.10:g.32383234C>G , CM000685.1:g.32383234C>G	GRCh37
NC_000023.9:g.32293155C>G	NCBI36
NG_012232.1:g.979493G>C , LRG_199:g.979493G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357033.9:c.4928G>C MANE Select	ENSP00000354923.3:p.Gly1643Ala
ENST00000619831.5:c.896G>C	ENSP00000479270.2:p.Gly299Ala
ENST00000357033.8:c.4928G>C	ENSP00000354923.3:p.Gly1643Ala
ENST00000378677.6:c.4916G>C	ENSP00000367948.2:p.Gly1639Ala
ENST00000420596.5:c.176G>C	ENSP00000399897.1:p.Gly59Ala
ENST00000448370.5:c.94-407G>C	ENSP00000388559.1:n.94-407G>C
ENST00000488902.5:n.336-148054G>C
ENST00000619831.4:c.4916G>C	ENSP00000479270.1:p.Gly1639Ala
ENST00000620040.4:c.4928G>C	ENSP00000478150.1:p.Gly1643Ala
NM_000109.3:c.4904G>C	NP_000100.2:p.Gly1635Ala
NM_004006.2:c.4928G>C , LRG_199t1:c.4928G>C	NP_003997.1:p.Gly1643Ala
NM_004009.3:c.4916G>C	NP_004000.1:p.Gly1639Ala
NM_004010.3:c.4559G>C	NP_004001.1:p.Gly1520Ala
NM_004011.3:c.905G>C	NP_004002.2:p.Gly302Ala
NM_004012.3:c.896G>C	NP_004003.1:p.Gly299Ala
XM_006724468.2:c.4928G>C	XP_006724531.1:p.Gly1643Ala
XM_006724469.2:c.4904G>C	XP_006724532.1:p.Gly1635Ala
XM_006724470.2:c.4928G>C	XP_006724533.1:p.Gly1643Ala
XM_006724471.2:c.4928G>C	XP_006724534.1:p.Gly1643Ala
XM_006724472.2:c.4799G>C	XP_006724535.1:p.Gly1600Ala
XM_006724473.2:c.4928G>C	XP_006724536.1:p.Gly1643Ala
XM_006724474.2:c.4928G>C	XP_006724537.1:p.Gly1643Ala
XM_006724475.2:c.4928G>C	XP_006724538.1:p.Gly1643Ala
XM_011545467.1:c.4928G>C	XP_011543769.1:p.Gly1643Ala
XM_011545468.1:c.4928G>C	XP_011543770.1:p.Gly1643Ala
XM_011545469.1:c.4928G>C	XP_011543771.1:p.Gly1643Ala
XM_006724469.3:c.4904G>C	XP_006724532.1:p.Gly1635Ala
XM_006724470.3:c.4928G>C	XP_006724533.1:p.Gly1643Ala
XM_006724474.3:c.4928G>C	XP_006724537.1:p.Gly1643Ala
XM_011545468.2:c.4928G>C	XP_011543770.1:p.Gly1643Ala
XM_017029328.1:c.4928G>C	XP_016884817.1:p.Gly1643Ala
XM_017029329.1:c.4928G>C	XP_016884818.1:p.Gly1643Ala
XM_017029330.2:c.4928G>C	XP_016884819.1:p.Gly1643Ala
NM_000109.4:c.4904G>C	NP_000100.3:p.Gly1635Ala
NM_004006.3:c.4928G>C MANE Select	NP_003997.2:p.Gly1643Ala
NM_004011.4:c.905G>C	NP_004002.3:p.Gly302Ala
NM_004012.4:c.896G>C	NP_004003.2:p.Gly299Ala