Canonical Allele Identifier: CA169125766

Gene: ASB10

Linked Data

• dbSNP Id: rs104886490
• gnomAD v2: 7-150883947-C-T
• gnomAD v4: 7-151186860-C-T
• COSMIC: COSM3923178 ; COSM3923179 ; COSM3923180
• MyVariant Identifiers: chr7:g.150883947C>T (hg19) ; chr7:g.151186860C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186860C>T , CM000669.2:g.151186860C>T	GRCh38
NC_000007.13:g.150883947C>T , CM000669.1:g.150883947C>T	GRCh37
NC_000007.12:g.150514880C>T	NCBI36
NG_017016.1:g.5973G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.271G>A MANE Select	ENSP00000391137.2:p.Asp91Asn
ENST00000275838.5:c.271G>A	ENSP00000275838.1:p.Asp91Asn
ENST00000377867.7:c.272-201G>A	ENSP00000367098.3:n.272-201G>A
ENST00000415615.1:c.*315G>A	ENSP00000410871.1:n.*315G>A
ENST00000420175.2:c.271G>A	ENSP00000391137.2:p.Asp91Asn
NM_001142459.1:c.271G>A	NP_001135931.2:p.Asp91Asn
NM_001142460.1:c.271G>A	NP_001135932.2:p.Asp91Asn
NM_080871.3:c.272-201G>A	NP_543147.2:n.272-201G>A
XM_005249949.3:c.406G>A	XP_005250006.1:p.Asp136Asn
NM_001142459.2:c.271G>A MANE Select	NP_001135931.2:p.Asp91Asn
NM_080871.4:c.272-201G>A	NP_543147.2:n.272-201G>A