Canonical Allele Identifier: CA1726201162
Gene: SAMD9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93103948A= , CM000669.2:g.93103948A= GRCh38
NC_000007.13:g.92733261A= , CM000669.1:g.92733261A= GRCh37
NC_000007.12:g.92571197A= NCBI36
NG_023419.1:g.19076T=

Transcript Alleles

HGVS Amino-acid change
ENST00000379958.3:c.2150T= MANE Select ENSP00000369292.2:p.Met717=
ENST00000379958.2:c.2150T= ENSP00000369292.2:p.Met717=
ENST00000446617.1:c.2150T= ENSP00000414529.1:p.Met717=
ENST00000620985.4:c.2150T= ENSP00000484636.1:p.Met717=
NM_001193307.1:c.2150T= NP_001180236.1:p.Met717=
NM_017654.3:c.2150T= NP_060124.2:p.Met717=
NM_017654.4:c.2150T= MANE Select NP_060124.2:p.Met717=
NM_001193307.2:c.2150T= NP_001180236.1:p.Met717=