Canonical Allele Identifier: CA370037807

Gene: ASB10

Linked Data

• MyVariant Identifiers: chr7:g.150884098C>G (hg19) ; chr7:g.151187011C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187011C>G , CM000669.2:g.151187011C>G	GRCh38
NC_000007.13:g.150884098C>G , CM000669.1:g.150884098C>G	GRCh37
NC_000007.12:g.150515031C>G	NCBI36
NG_017016.1:g.5822G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.120G>C MANE Select	ENSP00000391137.2:p.Lys40Asn
ENST00000275838.5:c.120G>C	ENSP00000275838.1:p.Lys40Asn
ENST00000377867.7:c.272-352G>C	ENSP00000367098.3:n.272-352G>C
ENST00000415615.1:c.*164G>C	ENSP00000410871.1:n.*164G>C
ENST00000420175.2:c.120G>C	ENSP00000391137.2:p.Lys40Asn
NM_001142459.1:c.120G>C	NP_001135931.2:p.Lys40Asn
NM_001142460.1:c.120G>C	NP_001135932.2:p.Lys40Asn
NM_080871.3:c.272-352G>C	NP_543147.2:n.272-352G>C
XM_005249949.3:c.255G>C	XP_005250006.1:p.Lys85Asn
NM_001142459.2:c.120G>C MANE Select	NP_001135931.2:p.Lys40Asn
NM_080871.4:c.272-352G>C	NP_543147.2:n.272-352G>C