Canonical Allele Identifier: CA448522197

Gene: DSP

Linked Data

• MyVariant Identifiers: chr6:g.7568808del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7568575del , CM000668.2:g.7568575del	GRCh38
NC_000006.11:g.7568808del , CM000668.1:g.7568808del	GRCh37
NC_000006.10:g.7513807del	NCBI36
NG_008803.1:g.31939del , LRG_423:g.31939del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.1405del	ENSP00000518230.1:p.Tyr469ThrfsTer16
ENST00000379802.8:c.1405del MANE Select	ENSP00000369129.3:p.Tyr469ThrfsTer16
ENST00000379802.7:c.1405del	ENSP00000369129.3:p.Tyr469ThrfsTer16
ENST00000418664.2:c.1405del	ENSP00000396591.2:p.Tyr469ThrfsTer16
NM_001008844.1:c.1405del	NP_001008844.1:p.Tyr469ThrfsTer16
NM_004415.2:c.1405del , LRG_423t1:c.1405del	NP_004406.2:p.Tyr469ThrfsTer16
XM_011514323.1:c.1405del	XP_011512625.1:p.Tyr469ThrfsTer16
NM_001008844.2:c.1405del	NP_001008844.1:p.Tyr469ThrfsTer16
NM_001319034.1:c.1405del	NP_001305963.1:p.Tyr469ThrfsTer16
NM_004415.3:c.1405del	NP_004406.2:p.Tyr469ThrfsTer16
NM_004415.4:c.1405del MANE Select	NP_004406.2:p.Tyr469ThrfsTer16
NM_001008844.3:c.1405del	NP_001008844.1:p.Tyr469ThrfsTer16
NM_001319034.2:c.1405del	NP_001305963.1:p.Tyr469ThrfsTer16