Canonical Allele Identifier: CA133956153

Gene: DSP

Linked Data

• dbSNP Id: rs891747155
• gnomAD v3: 6-7568726-ATG-A
• gnomAD v4: 6-7568726-ATG-A
• MyVariant Identifiers: chr6:g.7568960_7568961del (hg19) ; chr6:g.7568727_7568728del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7568727_7568728del , CM000668.2:g.7568727_7568728del	GRCh38
NC_000006.11:g.7568960_7568961del , CM000668.1:g.7568960_7568961del	GRCh37
NC_000006.10:g.7513959_7513960del	NCBI36
NG_008803.1:g.32091_32092del , LRG_423:g.32091_32092del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.1419+138_1419+139del	ENSP00000518230.1:n.1419+138_1419+139del
ENST00000379802.8:c.1419+138_1419+139del MANE Select	ENSP00000369129.3:n.1419+138_1419+139del
ENST00000379802.7:c.1419+138_1419+139del	ENSP00000369129.3:n.1419+138_1419+139del
ENST00000418664.2:c.1419+138_1419+139del	ENSP00000396591.2:n.1419+138_1419+139del
NM_001008844.1:c.1419+138_1419+139del	NP_001008844.1:n.1419+138_1419+139del
NM_004415.2:c.1419+138_1419+139del , LRG_423t1:c.1419+138_1419+139del	NP_004406.2:n.1419+138_1419+139del
XM_011514323.1:c.1419+138_1419+139del	XP_011512625.1:n.1419+138_1419+139del
NM_001008844.2:c.1419+138_1419+139del	NP_001008844.1:n.1419+138_1419+139del
NM_001319034.1:c.1419+138_1419+139del	NP_001305963.1:n.1419+138_1419+139del
NM_004415.3:c.1419+138_1419+139del	NP_004406.2:n.1419+138_1419+139del
NM_004415.4:c.1419+138_1419+139del MANE Select	NP_004406.2:n.1419+138_1419+139del
NM_001008844.3:c.1419+138_1419+139del	NP_001008844.1:n.1419+138_1419+139del
NM_001319034.2:c.1419+138_1419+139del	NP_001305963.1:n.1419+138_1419+139del