Canonical Allele Identifier: CA370038091

Gene: ASB10

Linked Data

• gnomAD v4: 7-151187093-T-C
• MyVariant Identifiers: chr7:g.150884180T>C (hg19) ; chr7:g.151187093T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187093T>C , CM000669.2:g.151187093T>C	GRCh38
NC_000007.13:g.150884180T>C , CM000669.1:g.150884180T>C	GRCh37
NC_000007.12:g.150515113T>C	NCBI36
NG_017016.1:g.5740A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.38A>G MANE Select	ENSP00000391137.2:p.Gln13Arg
ENST00000275838.5:c.38A>G	ENSP00000275838.1:p.Gln13Arg
ENST00000377867.7:c.271+359A>G	ENSP00000367098.3:n.271+359A>G
ENST00000415615.1:c.*122-40A>G	ENSP00000410871.1:n.*122-40A>G
ENST00000420175.2:c.38A>G	ENSP00000391137.2:p.Gln13Arg
NM_001142459.1:c.38A>G	NP_001135931.2:p.Gln13Arg
NM_001142460.1:c.38A>G	NP_001135932.2:p.Gln13Arg
NM_080871.3:c.271+359A>G	NP_543147.2:n.271+359A>G
XM_005249949.3:c.173A>G	XP_005250006.1:p.Gln58Arg
NM_001142459.2:c.38A>G MANE Select	NP_001135931.2:p.Gln13Arg
NM_080871.4:c.271+359A>G	NP_543147.2:n.271+359A>G