Canonical Allele Identifier: CA2695206017

Gene: DSP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7585131_7585132insA , CM000668.2:g.7585131_7585132insA	GRCh38
NC_000006.11:g.7585364_7585365insA , CM000668.1:g.7585364_7585365insA	GRCh37
NC_000006.10:g.7530363_7530364insA	NCBI36
NG_008803.1:g.48495_48496insA , LRG_423:g.48495_48496insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.6540_6541insA	ENSP00000518230.1:p.Asp2181ArgfsTer20
ENST00000379802.8:c.7869_7870insA MANE Select	ENSP00000369129.3:p.Asp2624ArgfsTer20
ENST00000379802.7:c.7869_7870insA	ENSP00000369129.3:p.Asp2624ArgfsTer20
ENST00000418664.2:c.6072_6073insA	ENSP00000396591.2:p.Asp2025ArgfsTer20
NM_001008844.1:c.6072_6073insA	NP_001008844.1:p.Asp2025ArgfsTer20
NM_004415.2:c.7869_7870insA , LRG_423t1:c.7869_7870insA	NP_004406.2:p.Asp2624ArgfsTer20
XM_011514323.1:c.6540_6541insA	XP_011512625.1:p.Asp2181ArgfsTer20
NM_001008844.2:c.6072_6073insA	NP_001008844.1:p.Asp2025ArgfsTer20
NM_001319034.1:c.6540_6541insA	NP_001305963.1:p.Asp2181ArgfsTer20
NM_004415.3:c.7869_7870insA	NP_004406.2:p.Asp2624ArgfsTer20
NM_004415.4:c.7869_7870insA MANE Select	NP_004406.2:p.Asp2624ArgfsTer20
NM_001008844.3:c.6072_6073insA	NP_001008844.1:p.Asp2025ArgfsTer20
NM_001319034.2:c.6540_6541insA	NP_001305963.1:p.Asp2181ArgfsTer20