Canonical Allele Identifier: CA368176666

Gene: SAMD9

Linked Data

• MyVariant Identifiers: chr7:g.92730748G>T (hg19) ; chr7:g.93101435G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93101435G>T , CM000669.2:g.93101435G>T	GRCh38
NC_000007.13:g.92730748G>T , CM000669.1:g.92730748G>T	GRCh37
NC_000007.12:g.92568684G>T	NCBI36
NG_023419.1:g.21589C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379958.3:c.4663C>A MANE Select	ENSP00000369292.2:p.Pro1555Thr
ENST00000379958.2:c.4663C>A	ENSP00000369292.2:p.Pro1555Thr
ENST00000620985.4:c.4663C>A	ENSP00000484636.1:p.Pro1555Thr
NM_001193307.1:c.4663C>A	NP_001180236.1:p.Pro1555Thr
NM_017654.3:c.4663C>A	NP_060124.2:p.Pro1555Thr
NM_017654.4:c.4663C>A MANE Select	NP_060124.2:p.Pro1555Thr
NM_001193307.2:c.4663C>A	NP_001180236.1:p.Pro1555Thr