Canonical Allele Identifier: CA2259411612

Gene: MSL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40132750A>T , CM000679.2:g.40132750A>T	GRCh38
NC_000017.10:g.38289003A>T , CM000679.1:g.38289003A>T	GRCh37
NC_000017.9:g.35542529A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398532.9:c.1489-292A>T MANE Select	ENSP00000381543.3:n.1489-292A>T
ENST00000339569.9:n.650-292A>T
ENST00000398532.8:c.1489-292A>T	ENSP00000381543.3:n.1489-292A>T
ENST00000578648.5:c.1441-292A>T	ENSP00000462731.1:n.1441-292A>T
ENST00000579565.5:c.700-292A>T	ENSP00000462945.1:n.700-292A>T
ENST00000580086.1:n.109-292A>T
ENST00000581246.5:n.530-292A>T
ENST00000583127.1:n.320-292A>T
NM_001012241.1:c.700-292A>T	NP_001012241.1:n.700-292A>T
XM_005257298.3:c.1489-292A>T	XP_005257355.1:n.1489-292A>T
XM_005257299.3:c.838-292A>T	XP_005257356.2:n.838-292A>T
XM_011524740.1:c.154-292A>T	XP_011523042.1:n.154-292A>T
NM_001012241.2:c.700-292A>T	NP_001012241.1:n.700-292A>T
NM_001365919.1:c.1489-292A>T MANE Select	NP_001352848.1:n.1489-292A>T
NM_001365920.1:c.1441-292A>T	NP_001352849.1:n.1441-292A>T