Canonical Allele Identifier: CA368176549

Gene: SAMD9

Linked Data

• MyVariant Identifiers: chr7:g.92730740A>C (hg19) ; chr7:g.93101427A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93101427A>C , CM000669.2:g.93101427A>C	GRCh38
NC_000007.13:g.92730740A>C , CM000669.1:g.92730740A>C	GRCh37
NC_000007.12:g.92568676A>C	NCBI36
NG_023419.1:g.21597T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379958.3:c.4671T>G MANE Select	ENSP00000369292.2:p.Phe1557Leu
ENST00000379958.2:c.4671T>G	ENSP00000369292.2:p.Phe1557Leu
ENST00000620985.4:c.4671T>G	ENSP00000484636.1:p.Phe1557Leu
NM_001193307.1:c.4671T>G	NP_001180236.1:p.Phe1557Leu
NM_017654.3:c.4671T>G	NP_060124.2:p.Phe1557Leu
NM_017654.4:c.4671T>G MANE Select	NP_060124.2:p.Phe1557Leu
NM_001193307.2:c.4671T>G	NP_001180236.1:p.Phe1557Leu