Canonical Allele Identifier: CA828074095

Gene: DSP

Linked Data

• dbSNP Id: rs1468884598
• gnomAD v3: 6-7565261-T-TG
• gnomAD v4: 6-7565261-T-TG
• MyVariant Identifiers: chr6:g.7565494_7565495insG (hg19) ; chr6:g.7565261_7565262insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7565261_7565262insG , CM000668.2:g.7565261_7565262insG	GRCh38
NC_000006.11:g.7565494_7565495insG , CM000668.1:g.7565494_7565495insG	GRCh37
NC_000006.10:g.7510493_7510494insG	NCBI36
NG_008803.1:g.28625_28626insG , LRG_423:g.28625_28626insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710359.1:c.778-98_778-97insG	ENSP00000518230.1:n.778-98_778-97insG
ENST00000682228.1:n.4_5insG
ENST00000379802.8:c.778-98_778-97insG MANE Select	ENSP00000369129.3:n.778-98_778-97insG
ENST00000379802.7:c.778-98_778-97insG	ENSP00000369129.3:n.778-98_778-97insG
ENST00000418664.2:c.778-98_778-97insG	ENSP00000396591.2:n.778-98_778-97insG
ENST00000506617.1:n.296-98_296-97insG
NM_001008844.1:c.778-98_778-97insG	NP_001008844.1:n.778-98_778-97insG
NM_004415.2:c.778-98_778-97insG , LRG_423t1:c.778-98_778-97insG	NP_004406.2:n.778-98_778-97insG
XM_011514323.1:c.778-98_778-97insG	XP_011512625.1:n.778-98_778-97insG
NM_001008844.2:c.778-98_778-97insG	NP_001008844.1:n.778-98_778-97insG
NM_001319034.1:c.778-98_778-97insG	NP_001305963.1:n.778-98_778-97insG
NM_004415.3:c.778-98_778-97insG	NP_004406.2:n.778-98_778-97insG
NM_004415.4:c.778-98_778-97insG MANE Select	NP_004406.2:n.778-98_778-97insG
NM_001008844.3:c.778-98_778-97insG	NP_001008844.1:n.778-98_778-97insG
NM_001319034.2:c.778-98_778-97insG	NP_001305963.1:n.778-98_778-97insG