Canonical Allele Identifier: CA14734982

Gene: MAU2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.19333177T>C , CM000681.2:g.19333177T>C	GRCh38
NC_000019.9:g.19443986T>C , CM000681.1:g.19443986T>C	GRCh37
NC_000019.8:g.19304986T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262815.13:c.277-2541T>C MANE Select	ENSP00000262815.9:n.277-2541T>C
ENST00000262815.12:c.277-2541T>C	ENSP00000262815.9:n.277-2541T>C
ENST00000586189.7:n.380-2541T>C
ENST00000609122.5:c.151-3993T>C	ENSP00000477034.1:n.151-3993T>C
NM_015329.3:c.277-2541T>C	NP_056144.3:n.277-2541T>C
XM_005259837.2:c.277-2541T>C	XP_005259894.2:n.277-2541T>C
XM_005259838.2:c.277-3993T>C	XP_005259895.2:n.277-3993T>C
XM_006722711.2:c.277-2541T>C	XP_006722774.2:n.277-2541T>C
XM_011527843.1:c.28-2541T>C	XP_011526145.1:n.28-2541T>C
XM_011527844.1:c.-300-2541T>C	XP_011526146.1:n.-300-2541T>C
XR_430132.2:n.308-2541T>C
XM_005259837.3:c.277-2541T>C	XP_005259894.2:n.277-2541T>C
XM_005259838.4:c.394-3993T>C	XP_005259895.3:n.394-3993T>C
XM_006722711.3:c.277-2541T>C	XP_006722774.2:n.277-2541T>C
XM_011527844.2:c.-300-2541T>C	XP_011526146.1:n.-300-2541T>C
XM_017026539.2:c.394-3993T>C	XP_016882028.1:n.394-3993T>C
NM_015329.4:c.277-2541T>C MANE Select	NP_056144.3:n.277-2541T>C