Canonical Allele Identifier: CA579181

Gene: NMNAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.9975675G>T , CM000663.2:g.9975675G>T	GRCh38
NC_000001.10:g.10035733G>T , CM000663.1:g.10035733G>T	GRCh37
NC_000001.9:g.9958320G>T	NCBI36
NG_032954.1:g.37248G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_022787.4:c.199G>T MANE Select	NP_073624.2:p.Val67Phe
ENST00000377205.6:c.199G>T MANE Select	ENSP00000366410.1:p.Val67Phe
NM_001297778.1:c.199G>T	NP_001284707.1:p.Val67Phe
NM_001297779.1:c.199G>T	NP_001284708.1:p.Val67Phe
NM_001297779.2:c.199G>T	NP_001284708.1:p.Val67Phe
NM_022787.3:c.199G>T	NP_073624.2:p.Val67Phe
ENST00000377205.5:c.199G>T	ENSP00000366410.1:p.Val67Phe
ENST00000403197.5:c.199G>T	ENSP00000385131.1:p.Val67Phe
ENST00000462686.1:c.199G>T	ENSP00000435134.1:p.Val67Phe
XM_011541971.1:c.199G>T	XP_011540273.1:p.Val67Phe
XM_011541971.2:c.199G>T	XP_011540273.1:p.Val67Phe
XM_017002107.2:c.199G>T	XP_016857596.1:p.Val67Phe
XM_017002108.2:c.199G>T	XP_016857597.1:p.Val67Phe