Canonical Allele Identifier: CA913124319

Gene: ASB10

Linked Data

• gnomAD v4: 7-151187151-G-A
• MyVariant Identifiers: chr7:g.150884238G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187151G>A , CM000669.2:g.151187151G>A	GRCh38
NC_000007.13:g.150884238G>A , CM000669.1:g.150884238G>A	GRCh37
NC_000007.12:g.150515171G>A	NCBI36
NG_017016.1:g.5682C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.-21C>T MANE Select	ENSP00000391137.2:n.-21C>T
ENST00000275838.5:c.-21C>T	ENSP00000275838.1:n.-21C>T
ENST00000377867.7:c.271+301C>T	ENSP00000367098.3:n.271+301C>T
ENST00000415615.1:c.*122-98C>T	ENSP00000410871.1:n.*122-98C>T
ENST00000420175.2:c.-21C>T	ENSP00000391137.2:n.-21C>T
NM_001142459.1:c.-21C>T	NP_001135931.2:n.-21C>T
NM_001142460.1:c.-21C>T	NP_001135932.2:n.-21C>T
NM_080871.3:c.271+301C>T	NP_543147.2:n.271+301C>T
XM_005249949.3:c.115C>T	XP_005250006.1:p.His39Tyr
NM_001142459.2:c.-21C>T MANE Select	NP_001135931.2:n.-21C>T
NM_080871.4:c.271+301C>T	NP_543147.2:n.271+301C>T