Canonical Allele Identifier: CA565358247

Gene: DSP

Linked Data

• dbSNP Id: rs1264468970
• gnomAD v2: 6-7565497-T-TTTTTA
• gnomAD v3: 6-7565264-T-TTTTTA
• gnomAD v4: 6-7565264-T-TTTTTA
• MyVariant Identifiers: chr6:g.7565497_7565498insTTTTA (hg19) ; chr6:g.7565264_7565265insTTTTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7565267_7565268insTATTT , CM000668.2:g.7565267_7565268insTATTT	GRCh38
NC_000006.11:g.7565500_7565501insTATTT , CM000668.1:g.7565500_7565501insTATTT	GRCh37
NC_000006.10:g.7510499_7510500insTATTT	NCBI36
NG_008803.1:g.28631_28632insTATTT , LRG_423:g.28631_28632insTATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.778-92_778-91insTATTT	ENSP00000518230.1:n.778-92_778-91insTATTT
ENST00000682228.1:n.10_11insTATTT
ENST00000379802.8:c.778-92_778-91insTATTT MANE Select	ENSP00000369129.3:n.778-92_778-91insTATTT
ENST00000379802.7:c.778-92_778-91insTATTT	ENSP00000369129.3:n.778-92_778-91insTATTT
ENST00000418664.2:c.778-92_778-91insTATTT	ENSP00000396591.2:n.778-92_778-91insTATTT
ENST00000506617.1:n.296-92_296-91insTATTT
NM_001008844.1:c.778-92_778-91insTATTT	NP_001008844.1:n.778-92_778-91insTATTT
NM_004415.2:c.778-92_778-91insTATTT , LRG_423t1:c.778-92_778-91insTATTT	NP_004406.2:n.778-92_778-91insTATTT
XM_011514323.1:c.778-92_778-91insTATTT	XP_011512625.1:n.778-92_778-91insTATTT
NM_001008844.2:c.778-92_778-91insTATTT	NP_001008844.1:n.778-92_778-91insTATTT
NM_001319034.1:c.778-92_778-91insTATTT	NP_001305963.1:n.778-92_778-91insTATTT
NM_004415.3:c.778-92_778-91insTATTT	NP_004406.2:n.778-92_778-91insTATTT
NM_004415.4:c.778-92_778-91insTATTT MANE Select	NP_004406.2:n.778-92_778-91insTATTT
NM_001008844.3:c.778-92_778-91insTATTT	NP_001008844.1:n.778-92_778-91insTATTT
NM_001319034.2:c.778-92_778-91insTATTT	NP_001305963.1:n.778-92_778-91insTATTT