Canonical Allele Identifier: CA2841094046

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585905C>A , CM000668.2:g.7585905C>A	GRCh38
NC_000006.11:g.7586138C>A , CM000668.1:g.7586138C>A	GRCh37
NC_000006.10:g.7531137C>A	NCBI36
NG_008803.1:g.49269C>A , LRG_423:g.49269C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.*27C>A	ENSP00000518230.1:n.*27C>A
ENST00000379802.8:c.*27C>A MANE Select	ENSP00000369129.3:n.*27C>A
ENST00000379802.7:c.*27C>A	ENSP00000369129.3:n.*27C>A
ENST00000418664.2:c.*27C>A	ENSP00000396591.2:n.*27C>A
NM_001008844.1:c.*27C>A	NP_001008844.1:n.*27C>A
NM_004415.2:c.*27C>A , LRG_423t1:c.*27C>A	NP_004406.2:n.*27C>A
XM_011514323.1:c.*27C>A	XP_011512625.1:n.*27C>A
NM_001008844.2:c.*27C>A	NP_001008844.1:n.*27C>A
NM_001319034.1:c.*27C>A	NP_001305963.1:n.*27C>A
NM_004415.3:c.*27C>A	NP_004406.2:n.*27C>A
NM_004415.4:c.*27C>A MANE Select	NP_004406.2:n.*27C>A
NM_001008844.3:c.*27C>A	NP_001008844.1:n.*27C>A
NM_001319034.2:c.*27C>A	NP_001305963.1:n.*27C>A