Canonical Allele Identifier: CA8741533

Gene: MTNAP1 CPSF4L

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.73247312G>A , CM000679.2:g.73247312G>A	GRCh38
NC_000017.10:g.71243451G>A , CM000679.1:g.71243451G>A	GRCh37
NC_000017.9:g.68755046G>A	NCBI36
NG_054938.1:g.20223G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001351264.2:c.1801G>A (MTNAP1) MANE Select	NP_001338193.2:p.Asp601Asn
ENST00000535032.7:c.1801G>A (MTNAP1) MANE Select	ENSP00000440551.2:p.Asp601Asn
NM_001100621.2:c.1693G>A (MTNAP1)	NP_001094091.1:p.Asp565Asn
NM_001100621.3:c.1693G>A (MTNAP1)	NP_001094091.2:p.Asp565Asn
NM_001288770.1:c.1693G>A (MTNAP1)	NP_001275699.1:p.Asp565Asn
NM_001288770.2:c.1693G>A (MTNAP1)	NP_001275699.1:p.Asp565Asn
NM_001288770.3:c.1693G>A (MTNAP1)	NP_001275699.2:p.Asp565Asn
NM_001351264.1:c.1801G>A (MTNAP1)	NP_001338193.1:p.Asp601Asn
NM_001351265.1:c.1693G>A (MTNAP1)	NP_001338194.1:p.Asp565Asn
NM_001351265.2:c.1693G>A (MTNAP1)	NP_001338194.2:p.Asp565Asn
NM_017941.5:c.1801G>A (MTNAP1)	NP_060411.2:p.Asp601Asn
NM_017941.6:c.1801G>A (MTNAP1)	NP_060411.3:p.Asp601Asn
NR_110105.1:n.490G>A (MTNAP1)
NR_110105.2:n.451G>A (MTNAP1)
ENST00000268942.12:c.1693G>A (MTNAP1)	ENSP00000268942.8:p.Asp565Asn
ENST00000359042.6:c.1801G>A (MTNAP1)	ENSP00000351937.2:p.Asp601Asn
ENST00000535032.6:c.1801G>A (MTNAP1)	ENSP00000440551.2:p.Asp601Asn
ENST00000577615.5:c.1693G>A (MTNAP1)	ENSP00000464132.1:p.Asp565Asn
ENST00000582793.1:c.208G>A (MTNAP1)	ENSP00000463718.1:p.Asp70Asn
XM_005257487.3:c.1801G>A (MTNAP1)	XP_005257544.1:p.Asp601Asn
XM_011524961.1:c.1801G>A (MTNAP1)	XP_011523263.1:p.Asp601Asn
XM_011524962.1:c.1801G>A (MTNAP1)	XP_011523264.1:p.Asp601Asn
XM_011524962.2:c.1801G>A (MTNAP1)	XP_011523264.1:p.Asp601Asn
XM_011525115.1:c.564-4880C>T (CPSF4L)	XP_011523417.1:n.564-4880C>T
XM_011525115.2:c.564-4880C>T (CPSF4L)	XP_011523417.1:n.564-4880C>T