Canonical Allele Identifier: CA029968

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7555721A>G , CM000668.2:g.7555721A>G	GRCh38
NC_000006.11:g.7555954A>G , CM000668.1:g.7555954A>G	GRCh37
NC_000006.10:g.7500953A>G	NCBI36
NG_008803.1:g.19085A>G , LRG_423:g.19085A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004415.4:c.174A>G MANE Select	NP_004406.2:p.Gln58=
ENST00000379802.8:c.174A>G MANE Select	ENSP00000369129.3:p.Gln58=
NM_001008844.1:c.174A>G	NP_001008844.1:p.Gln58=
NM_001008844.2:c.174A>G	NP_001008844.1:p.Gln58=
NM_001008844.3:c.174A>G	NP_001008844.1:p.Gln58=
NM_001319034.1:c.174A>G	NP_001305963.1:p.Gln58=
NM_001319034.2:c.174A>G	NP_001305963.1:p.Gln58=
NM_004415.2:c.174A>G , LRG_423t1:c.174A>G	NP_004406.2:p.Gln58=
NM_004415.3:c.174A>G	NP_004406.2:p.Gln58=
ENST00000379802.7:c.174A>G	ENSP00000369129.3:p.Gln58=
ENST00000418664.2:c.174A>G	ENSP00000396591.2:p.Gln58=
ENST00000683563.1:n.66A>G
ENST00000683682.1:c.69A>G	ENSP00000508162.1:p.Gln23=
ENST00000683682.2:c.174A>G	ENSP00000508162.2:p.Gln58=
ENST00000710359.1:c.174A>G	ENSP00000518230.1:p.Gln58=
XM_011514323.1:c.174A>G	XP_011512625.1:p.Gln58=