Canonical Allele Identifier: CA362687069

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7580937A>T , CM000668.2:g.7580937A>T	GRCh38
NC_000006.11:g.7581170A>T , CM000668.1:g.7581170A>T	GRCh37
NC_000006.10:g.7526169A>T	NCBI36
NG_008803.1:g.44301A>T , LRG_423:g.44301A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004415.4:c.4747A>T MANE Select	NP_004406.2:p.Thr1583Ser
ENST00000379802.8:c.4747A>T MANE Select	ENSP00000369129.3:p.Thr1583Ser
NM_001008844.1:c.3582+1165A>T	NP_001008844.1:n.3582+1165A>T
NM_001008844.2:c.3582+1165A>T	NP_001008844.1:n.3582+1165A>T
NM_001008844.3:c.3582+1165A>T	NP_001008844.1:n.3582+1165A>T
NM_001319034.1:c.4050+697A>T	NP_001305963.1:n.4050+697A>T
NM_001319034.2:c.4050+697A>T	NP_001305963.1:n.4050+697A>T
NM_004415.2:c.4747A>T , LRG_423t1:c.4747A>T	NP_004406.2:p.Thr1583Ser
NM_004415.3:c.4747A>T	NP_004406.2:p.Thr1583Ser
ENST00000379802.7:c.4747A>T	ENSP00000369129.3:p.Thr1583Ser
ENST00000418664.2:c.3582+1165A>T	ENSP00000396591.2:n.3582+1165A>T
ENST00000710359.1:c.4050+697A>T	ENSP00000518230.1:n.4050+697A>T
XM_011514323.1:c.4050+697A>T	XP_011512625.1:n.4050+697A>T