Canonical Allele Identifier: CA370038159

Gene: ASB10

Linked Data

• gnomAD v4: 7-151187112-G-T
• MyVariant Identifiers: chr7:g.150884199G>T (hg19) ; chr7:g.151187112G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187112G>T , CM000669.2:g.151187112G>T	GRCh38
NC_000007.13:g.150884199G>T , CM000669.1:g.150884199G>T	GRCh37
NC_000007.12:g.150515132G>T	NCBI36
NG_017016.1:g.5721C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.19C>A MANE Select	ENSP00000391137.2:p.Pro7Thr
ENST00000275838.5:c.19C>A	ENSP00000275838.1:p.Pro7Thr
ENST00000377867.7:c.271+340C>A	ENSP00000367098.3:n.271+340C>A
ENST00000415615.1:c.*122-59C>A	ENSP00000410871.1:n.*122-59C>A
ENST00000420175.2:c.19C>A	ENSP00000391137.2:p.Pro7Thr
NM_001142459.1:c.19C>A	NP_001135931.2:p.Pro7Thr
NM_001142460.1:c.19C>A	NP_001135932.2:p.Pro7Thr
NM_080871.3:c.271+340C>A	NP_543147.2:n.271+340C>A
XM_005249949.3:c.154C>A	XP_005250006.1:p.Pro52Thr
NM_001142459.2:c.19C>A MANE Select	NP_001135931.2:p.Pro7Thr
NM_080871.4:c.271+340C>A	NP_543147.2:n.271+340C>A