Canonical Allele Identifier: CA2572105955

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7565733dup , CM000668.2:g.7565733dup	GRCh38
NC_000006.11:g.7565966dup , CM000668.1:g.7565966dup	GRCh37
NC_000006.10:g.7510965dup	NCBI36
NG_008803.1:g.29097dup , LRG_423:g.29097dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.939+213dup	ENSP00000518230.1:n.939+213dup
ENST00000682228.1:n.263+213dup
ENST00000379802.8:c.939+213dup MANE Select	ENSP00000369129.3:n.939+213dup
ENST00000379802.7:c.939+213dup	ENSP00000369129.3:n.939+213dup
ENST00000418664.2:c.939+213dup	ENSP00000396591.2:n.939+213dup
ENST00000506617.1:n.670dup
NM_001008844.1:c.939+213dup	NP_001008844.1:n.939+213dup
NM_004415.2:c.939+213dup , LRG_423t1:c.939+213dup	NP_004406.2:n.939+213dup
XM_011514323.1:c.939+213dup	XP_011512625.1:n.939+213dup
NM_001008844.2:c.939+213dup	NP_001008844.1:n.939+213dup
NM_001319034.1:c.939+213dup	NP_001305963.1:n.939+213dup
NM_004415.3:c.939+213dup	NP_004406.2:n.939+213dup
NM_004415.4:c.939+213dup MANE Select	NP_004406.2:n.939+213dup
NM_001008844.3:c.939+213dup	NP_001008844.1:n.939+213dup
NM_001319034.2:c.939+213dup	NP_001305963.1:n.939+213dup