Canonical Allele Identifier: CA362691394

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7583980C>A , CM000668.2:g.7583980C>A	GRCh38
NC_000006.11:g.7584213C>A , CM000668.1:g.7584213C>A	GRCh37
NC_000006.10:g.7529212C>A	NCBI36
NG_008803.1:g.47344C>A , LRG_423:g.47344C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004415.4:c.6718C>A MANE Select	NP_004406.2:p.Gln2240Lys
ENST00000379802.8:c.6718C>A MANE Select	ENSP00000369129.3:p.Gln2240Lys
NM_001008844.1:c.4921C>A	NP_001008844.1:p.Gln1641Lys
NM_001008844.2:c.4921C>A	NP_001008844.1:p.Gln1641Lys
NM_001008844.3:c.4921C>A	NP_001008844.1:p.Gln1641Lys
NM_001319034.1:c.5389C>A	NP_001305963.1:p.Gln1797Lys
NM_001319034.2:c.5389C>A	NP_001305963.1:p.Gln1797Lys
NM_004415.2:c.6718C>A , LRG_423t1:c.6718C>A	NP_004406.2:p.Gln2240Lys
NM_004415.3:c.6718C>A	NP_004406.2:p.Gln2240Lys
ENST00000379802.7:c.6718C>A	ENSP00000369129.3:p.Gln2240Lys
ENST00000418664.2:c.4921C>A	ENSP00000396591.2:p.Gln1641Lys
ENST00000710359.1:c.5389C>A	ENSP00000518230.1:p.Gln1797Lys
XM_011514323.1:c.5389C>A	XP_011512625.1:p.Gln1797Lys