Canonical Allele Identifier: CA370034653
Gene: ASB10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.150878511C>A (hg19) chr7:g.151181424C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151181424C>A , CM000669.2:g.151181424C>A GRCh38
NC_000007.13:g.150878511C>A , CM000669.1:g.150878511C>A GRCh37
NC_000007.12:g.150509444C>A NCBI36
NG_017016.1:g.11409G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000420175.3:c.619G>T MANE Select ENSP00000391137.2:p.Val207Leu
ENST00000275838.5:c.619G>T ENSP00000275838.1:p.Val207Leu
ENST00000377867.7:c.574G>T ENSP00000367098.3:p.Val192Leu
ENST00000420175.2:c.619G>T ENSP00000391137.2:p.Val207Leu
NM_001142459.1:c.619G>T NP_001135931.2:p.Val207Leu
NM_001142460.1:c.619G>T NP_001135932.2:p.Val207Leu
NM_080871.3:c.574G>T NP_543147.2:p.Val192Leu
XM_005249949.3:c.754G>T XP_005250006.1:p.Val252Leu
NM_001142459.2:c.619G>T MANE Select NP_001135931.2:p.Val207Leu
NM_080871.4:c.574G>T NP_543147.2:p.Val192Leu
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