Canonical Allele Identifier: CA368178538
Gene: SAMD9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93101615T>A , CM000669.2:g.93101615T>A GRCh38
NC_000007.13:g.92730928T>A , CM000669.1:g.92730928T>A GRCh37
NC_000007.12:g.92568864T>A NCBI36
NG_023419.1:g.21409A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000379958.3:c.4483A>T MANE Select ENSP00000369292.2:p.Lys1495Ter
ENST00000379958.2:c.4483A>T ENSP00000369292.2:p.Lys1495Ter
ENST00000620985.4:c.4483A>T ENSP00000484636.1:p.Lys1495Ter
NM_001193307.1:c.4483A>T NP_001180236.1:p.Lys1495Ter
NM_017654.3:c.4483A>T NP_060124.2:p.Lys1495Ter
NM_017654.4:c.4483A>T MANE Select NP_060124.2:p.Lys1495Ter
NM_001193307.2:c.4483A>T NP_001180236.1:p.Lys1495Ter