Canonical Allele Identifier: CA707427690

Gene: MNAT1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.60841619T>A , CM000676.2:g.60841619T>A	GRCh38
NC_000014.8:g.61308337T>A , CM000676.1:g.61308337T>A	GRCh37
NC_000014.7:g.60378090T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261245.9:c.687+22772T>A MANE Select	ENSP00000261245.4:n.687+22772T>A
ENST00000261245.8:c.687+22772T>A	ENSP00000261245.4:n.687+22772T>A
ENST00000539616.6:c.561+29492T>A	ENSP00000446437.2:n.561+29492T>A
ENST00000554002.5:c.372+22772T>A	ENSP00000451379.1:n.372+22772T>A
ENST00000554641.1:n.268+22772T>A
ENST00000557134.1:c.267+22772T>A	ENSP00000451017.1:n.267+22772T>A
NM_001177963.1:c.561+29492T>A	NP_001171434.1:n.561+29492T>A
NM_002431.3:c.687+22772T>A	NP_002422.1:n.687+22772T>A
XM_005267687.1:c.687+22772T>A	XP_005267744.1:n.687+22772T>A
XM_005267688.1:c.687+22772T>A	XP_005267745.1:n.687+22772T>A
XM_011536795.1:c.324+22772T>A	XP_011535097.1:n.324+22772T>A
XM_005267687.3:c.687+22772T>A	XP_005267744.1:n.687+22772T>A
XM_005267688.3:c.687+22772T>A	XP_005267745.1:n.687+22772T>A
XM_017021332.2:c.642+22772T>A	XP_016876821.1:n.642+22772T>A
XM_017021333.2:c.324+22772T>A	XP_016876822.1:n.324+22772T>A
XM_017021334.2:c.324+22772T>A	XP_016876823.1:n.324+22772T>A
XM_024449599.1:c.324+22772T>A	XP_024305367.1:n.324+22772T>A
NM_002431.4:c.687+22772T>A MANE Select	NP_002422.1:n.687+22772T>A
NM_001177963.2:c.561+29492T>A	NP_001171434.1:n.561+29492T>A