Canonical Allele Identifier: CA565103817

Gene: DSP

Linked Data

• dbSNP Id: rs1443011576
• gnomAD v2: 6-7569337-ATC-A
• gnomAD v3: 6-7569104-ATC-A
• gnomAD v4: 6-7569104-ATC-A
• MyVariant Identifiers: chr6:g.7569338_7569339del (hg19) ; chr6:g.7569105_7569106del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7569108_7569109del , CM000668.2:g.7569108_7569109del	GRCh38
NC_000006.11:g.7569341_7569342del , CM000668.1:g.7569341_7569342del	GRCh37
NC_000006.10:g.7514340_7514341del	NCBI36
NG_008803.1:g.32472_32473del , LRG_423:g.32472_32473del

Transcript Alleles

HGVS	Amino-acid change
ENST00000710359.1:c.1420-78_1420-77del	ENSP00000518230.1:n.1420-78_1420-77del
ENST00000379802.8:c.1420-78_1420-77del MANE Select	ENSP00000369129.3:n.1420-78_1420-77del
ENST00000379802.7:c.1420-78_1420-77del	ENSP00000369129.3:n.1420-78_1420-77del
ENST00000418664.2:c.1420-78_1420-77del	ENSP00000396591.2:n.1420-78_1420-77del
NM_001008844.1:c.1420-78_1420-77del	NP_001008844.1:n.1420-78_1420-77del
NM_004415.2:c.1420-78_1420-77del , LRG_423t1:c.1420-78_1420-77del	NP_004406.2:n.1420-78_1420-77del
XM_011514323.1:c.1420-78_1420-77del	XP_011512625.1:n.1420-78_1420-77del
NM_001008844.2:c.1420-78_1420-77del	NP_001008844.1:n.1420-78_1420-77del
NM_001319034.1:c.1420-78_1420-77del	NP_001305963.1:n.1420-78_1420-77del
NM_004415.3:c.1420-78_1420-77del	NP_004406.2:n.1420-78_1420-77del
NM_004415.4:c.1420-78_1420-77del MANE Select	NP_004406.2:n.1420-78_1420-77del
NM_001008844.3:c.1420-78_1420-77del	NP_001008844.1:n.1420-78_1420-77del
NM_001319034.2:c.1420-78_1420-77del	NP_001305963.1:n.1420-78_1420-77del