Canonical Allele Identifier: CA1726201383

Gene: SAMD9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93104033_93104034delinsCT , CM000669.2:g.93104033_93104034delinsCT	GRCh38
NC_000007.13:g.92733346_92733347delinsCT , CM000669.1:g.92733346_92733347delinsCT	GRCh37
NC_000007.12:g.92571282_92571283delinsCT	NCBI36
NG_023419.1:g.18990_18991delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379958.3:c.2064_2065delinsAG MANE Select	ENSP00000369292.2:p.Lys688=
ENST00000379958.2:c.2064_2065delinsAG	ENSP00000369292.2:p.Lys688=
ENST00000446617.1:c.2064_2065delinsAG	ENSP00000414529.1:p.Lys688=
ENST00000620985.4:c.2064_2065delinsAG	ENSP00000484636.1:p.Lys688=
NM_001193307.1:c.2064_2065delinsAG	NP_001180236.1:p.Lys688=
NM_017654.3:c.2064_2065delinsAG	NP_060124.2:p.Lys688=
NM_017654.4:c.2064_2065delinsAG MANE Select	NP_060124.2:p.Lys688=
NM_001193307.2:c.2064_2065delinsAG	NP_001180236.1:p.Lys688=