Canonical Allele Identifier: CA368193397
Gene: SAMD9 HGNC NCBI

Linked Data

COSMIC: COSM230122

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93104027A>C , CM000669.2:g.93104027A>C GRCh38
NC_000007.13:g.92733340A>C , CM000669.1:g.92733340A>C GRCh37
NC_000007.12:g.92571276A>C NCBI36
NG_023419.1:g.18997T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000379958.3:c.2071T>G MANE Select ENSP00000369292.2:p.Trp691Gly
ENST00000379958.2:c.2071T>G ENSP00000369292.2:p.Trp691Gly
ENST00000446617.1:c.2071T>G ENSP00000414529.1:p.Trp691Gly
ENST00000620985.4:c.2071T>G ENSP00000484636.1:p.Trp691Gly
NM_001193307.1:c.2071T>G NP_001180236.1:p.Trp691Gly
NM_017654.3:c.2071T>G NP_060124.2:p.Trp691Gly
NM_017654.4:c.2071T>G MANE Select NP_060124.2:p.Trp691Gly
NM_001193307.2:c.2071T>G NP_001180236.1:p.Trp691Gly