Canonical Allele Identifier: CA565105477

Gene: DSP

Linked Data

• dbSNP Id: rs1355462341
• gnomAD v2: 6-7577291-A-ATTTTT
• gnomAD v4: 6-7577058-A-ATTTTT
• MyVariant Identifiers: chr6:g.7577291_7577292insTTTTT (hg19) ; chr6:g.7577058_7577059insTTTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7577058_7577059insTTTTT , CM000668.2:g.7577058_7577059insTTTTT	GRCh38
NC_000006.11:g.7577291_7577292insTTTTT , CM000668.1:g.7577291_7577292insTTTTT	GRCh37
NC_000006.10:g.7522290_7522291insTTTTT	NCBI36
NG_008803.1:g.40422_40423insTTTTT , LRG_423:g.40422_40423insTTTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000710359.1:c.2877+16_2877+17insTTTTT	ENSP00000518230.1:n.2877+16_2877+17insTTT...
ENST00000379802.8:c.2877+16_2877+17insTTTTT MANE Select	ENSP00000369129.3:n.2877+16_2877+17insTTT...
ENST00000379802.7:c.2877+16_2877+17insTTTTT	ENSP00000369129.3:n.2877+16_2877+17insTTT...
ENST00000418664.2:c.2877+16_2877+17insTTTTT	ENSP00000396591.2:n.2877+16_2877+17insTTT...
NM_001008844.1:c.2877+16_2877+17insTTTTT	NP_001008844.1:n.2877+16_2877+17insTTTTT
NM_004415.2:c.2877+16_2877+17insTTTTT , LRG_423t1:c.2877+16_2877+17insTTTTT	NP_004406.2:n.2877+16_2877+17insTTTTT
XM_011514323.1:c.2877+16_2877+17insTTTTT	XP_011512625.1:n.2877+16_2877+17insTTTTT
NM_001008844.2:c.2877+16_2877+17insTTTTT	NP_001008844.1:n.2877+16_2877+17insTTTTT
NM_001319034.1:c.2877+16_2877+17insTTTTT	NP_001305963.1:n.2877+16_2877+17insTTTTT
NM_004415.3:c.2877+16_2877+17insTTTTT	NP_004406.2:n.2877+16_2877+17insTTTTT
NM_004415.4:c.2877+16_2877+17insTTTTT MANE Select	NP_004406.2:n.2877+16_2877+17insTTTTT
NM_001008844.3:c.2877+16_2877+17insTTTTT	NP_001008844.1:n.2877+16_2877+17insTTTTT
NM_001319034.2:c.2877+16_2877+17insTTTTT	NP_001305963.1:n.2877+16_2877+17insTTTTT