Canonical Allele Identifier: CA362670845

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7555796G>A , CM000668.2:g.7555796G>A	GRCh38
NC_000006.11:g.7556029G>A , CM000668.1:g.7556029G>A	GRCh37
NC_000006.10:g.7501028G>A	NCBI36
NG_008803.1:g.19160G>A , LRG_423:g.19160G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004415.4:c.249G>A MANE Select	NP_004406.2:p.Met83Ile
ENST00000379802.8:c.249G>A MANE Select	ENSP00000369129.3:p.Met83Ile
NM_001008844.1:c.249G>A	NP_001008844.1:p.Met83Ile
NM_001008844.2:c.249G>A	NP_001008844.1:p.Met83Ile
NM_001008844.3:c.249G>A	NP_001008844.1:p.Met83Ile
NM_001319034.1:c.249G>A	NP_001305963.1:p.Met83Ile
NM_001319034.2:c.249G>A	NP_001305963.1:p.Met83Ile
NM_004415.2:c.249G>A , LRG_423t1:c.249G>A	NP_004406.2:p.Met83Ile
NM_004415.3:c.249G>A	NP_004406.2:p.Met83Ile
ENST00000379802.7:c.249G>A	ENSP00000369129.3:p.Met83Ile
ENST00000418664.2:c.249G>A	ENSP00000396591.2:p.Met83Ile
ENST00000683563.1:n.141G>A
ENST00000683682.1:c.144G>A	ENSP00000508162.1:p.Met48Ile
ENST00000683682.2:c.249G>A	ENSP00000508162.2:p.Met83Ile
ENST00000710359.1:c.249G>A	ENSP00000518230.1:p.Met83Ile
XM_011514323.1:c.249G>A	XP_011512625.1:p.Met83Ile