Canonical Allele Identifier: CA835247437

Gene: ASB10

Linked Data

• dbSNP Id: rs1172349988
• gnomAD v4: 7-151187213-G-T
• MyVariant Identifiers: chr7:g.150884300G>T (hg19) ; chr7:g.151187213G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187213G>T , CM000669.2:g.151187213G>T	GRCh38
NC_000007.13:g.150884300G>T , CM000669.1:g.150884300G>T	GRCh37
NC_000007.12:g.150515233G>T	NCBI36
NG_017016.1:g.5620C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.-83C>A MANE Select	ENSP00000391137.2:n.-83C>A
ENST00000275838.5:c.-83C>A	ENSP00000275838.1:n.-83C>A
ENST00000377867.7:c.271+239C>A	ENSP00000367098.3:n.271+239C>A
ENST00000415615.1:c.*121+41C>A	ENSP00000410871.1:n.*121+41C>A
NM_001142459.1:c.-83C>A	NP_001135931.2:n.-83C>A
NM_001142460.1:c.-83C>A	NP_001135932.2:n.-83C>A
NM_080871.3:c.271+239C>A	NP_543147.2:n.271+239C>A
XM_005249949.3:c.53C>A	XP_005250006.1:p.Ser18Tyr
NM_001142459.2:c.-83C>A MANE Select	NP_001135931.2:n.-83C>A
NM_080871.4:c.271+239C>A	NP_543147.2:n.271+239C>A