Canonical Allele Identifier: CA1608615020

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585593_7585594delinsCA , CM000668.2:g.7585593_7585594delinsCA	GRCh38
NC_000006.11:g.7585826_7585827delinsCA , CM000668.1:g.7585826_7585827delinsCA	GRCh37
NC_000006.10:g.7530825_7530826delinsCA	NCBI36
NG_008803.1:g.48957_48958delinsCA , LRG_423:g.48957_48958delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.7002_7003delinsCA	ENSP00000518230.1:p.Pro2334=
ENST00000379802.8:c.8331_8332delinsCA MANE Select	ENSP00000369129.3:p.Pro2777=
ENST00000379802.7:c.8331_8332delinsCA	ENSP00000369129.3:p.Pro2777=
ENST00000418664.2:c.6534_6535delinsCA	ENSP00000396591.2:p.Pro2178=
NM_001008844.1:c.6534_6535delinsCA	NP_001008844.1:p.Pro2178=
NM_004415.2:c.8331_8332delinsCA , LRG_423t1:c.8331_8332delinsCA	NP_004406.2:p.Pro2777=
XM_011514323.1:c.7002_7003delinsCA	XP_011512625.1:p.Pro2334=
NM_001008844.2:c.6534_6535delinsCA	NP_001008844.1:p.Pro2178=
NM_001319034.1:c.7002_7003delinsCA	NP_001305963.1:p.Pro2334=
NM_004415.3:c.8331_8332delinsCA	NP_004406.2:p.Pro2777=
NM_004415.4:c.8331_8332delinsCA MANE Select	NP_004406.2:p.Pro2777=
NM_001008844.3:c.6534_6535delinsCA	NP_001008844.1:p.Pro2178=
NM_001319034.2:c.7002_7003delinsCA	NP_001305963.1:p.Pro2334=