Canonical Allele Identifier: CA448529313

Gene: DSP DSP-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7542005G>A , CM000668.2:g.7542005G>A	GRCh38
NC_000006.11:g.7542238G>A , CM000668.1:g.7542238G>A	GRCh37
NC_000006.10:g.7487237G>A	NCBI36
NG_008803.1:g.5369G>A , LRG_423:g.5369G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004415.4:c.90G>A (DSP) MANE Select	NP_004406.2:p.Val30=
ENST00000379802.8:c.90G>A (DSP) MANE Select	ENSP00000369129.3:p.Val30=
NM_001008844.1:c.90G>A (DSP)	NP_001008844.1:p.Val30=
NM_001008844.2:c.90G>A (DSP)	NP_001008844.1:p.Val30=
NM_001008844.3:c.90G>A (DSP)	NP_001008844.1:p.Val30=
NM_001319034.1:c.90G>A (DSP)	NP_001305963.1:p.Val30=
NM_001319034.2:c.90G>A (DSP)	NP_001305963.1:p.Val30=
NM_004415.2:c.90G>A , LRG_423t1:c.90G>A (DSP)	NP_004406.2:p.Val30=
NM_004415.3:c.90G>A (DSP)	NP_004406.2:p.Val30=
ENST00000379802.7:c.90G>A (DSP)	ENSP00000369129.3:p.Val30=
ENST00000418664.2:c.90G>A (DSP)	ENSP00000396591.2:p.Val30=
ENST00000683682.2:c.90G>A (DSP)	ENSP00000508162.2:p.Val30=
ENST00000710359.1:c.90G>A (DSP)	ENSP00000518230.1:p.Val30=
XM_011514323.1:c.90G>A (DSP)	XP_011512625.1:p.Val30=
XR_241971.2:n.268+766C>T (DSP-AS1)
XR_241971.3:n.269+766C>T (DSP-AS1)