Canonical Allele Identifier: CA2679046371

Gene: MMUT

Linked Data

• gnomAD v4: 6-49447638-TAAAAAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49447649_49447654del , CM000668.2:g.49447649_49447654del	GRCh38
NC_000006.11:g.49415362_49415367del , CM000668.1:g.49415362_49415367del	GRCh37
NC_000006.10:g.49523321_49523326del	NCBI36
NG_007100.1:g.20496_20501del

Transcript Alleles

HGVS	Amino-acid change
ENST00000274813.4:c.1560+26_1560+31del MANE Select	ENSP00000274813.3:n.1560+26_1560+31del
ENST00000274813.3:c.1560+26_1560+31del	ENSP00000274813.3:n.1560+26_1560+31del
NM_000255.3:c.1560+26_1560+31del	NP_000246.2:n.1560+26_1560+31del
XM_005249143.2:c.1560+26_1560+31del	XP_005249200.1:n.1560+26_1560+31del
XM_005249143.3:c.1560+26_1560+31del	XP_005249200.1:n.1560+26_1560+31del
NM_000255.4:c.1560+26_1560+31del MANE Select	NP_000246.2:n.1560+26_1560+31del