Canonical Allele Identifier: CA370038221

Gene: ASB10

Linked Data

• MyVariant Identifiers: chr7:g.150884216A>T (hg19) ; chr7:g.151187129A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187129A>T , CM000669.2:g.151187129A>T	GRCh38
NC_000007.13:g.150884216A>T , CM000669.1:g.150884216A>T	GRCh37
NC_000007.12:g.150515149A>T	NCBI36
NG_017016.1:g.5704T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.2T>A MANE Select	ENSP00000391137.2:p.Met1Lys
ENST00000275838.5:c.2T>A	ENSP00000275838.1:p.Met1Lys
ENST00000377867.7:c.271+323T>A	ENSP00000367098.3:n.271+323T>A
ENST00000415615.1:c.*122-76T>A	ENSP00000410871.1:n.*122-76T>A
ENST00000420175.2:c.2T>A	ENSP00000391137.2:p.Met1Lys
NM_001142459.1:c.2T>A	NP_001135931.2:p.Met1Lys
NM_001142460.1:c.2T>A	NP_001135932.2:p.Met1Lys
NM_080871.3:c.271+323T>A	NP_543147.2:n.271+323T>A
XM_005249949.3:c.137T>A	XP_005250006.1:p.Met46Lys
NM_001142459.2:c.2T>A MANE Select	NP_001135931.2:p.Met1Lys
NM_080871.4:c.271+323T>A	NP_543147.2:n.271+323T>A