Canonical Allele Identifier: CA2677549489

Gene: GMNN

Linked Data

• gnomAD v4: 6-24777184-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24777186del , CM000668.2:g.24777186del	GRCh38
NC_000006.11:g.24777414del , CM000668.1:g.24777414del	GRCh37
NC_000006.10:g.24885393del	NCBI36
NG_030440.1:g.7256del

Transcript Alleles

HGVS	Amino-acid change
ENST00000230056.8:c.-25-36del MANE Select	ENSP00000230056.3:n.-25-36del
ENST00000230056.7:c.-25-36del	ENSP00000230056.3:n.-25-36del
ENST00000356509.7:c.-25-36del	ENSP00000348902.3:n.-25-36del
ENST00000378054.6:c.-25-36del	ENSP00000367293.2:n.-25-36del
ENST00000378059.3:c.-61del	ENSP00000367298.3:n.-61del
ENST00000468943.1:n.165-36del
ENST00000476555.5:c.-25-36del	ENSP00000419584.1:n.-25-36del
ENST00000620958.4:c.-25-36del	ENSP00000477506.1:n.-25-36del
NM_001251989.1:c.-25-36del	NP_001238918.1:n.-25-36del
NM_001251990.1:c.-25-36del	NP_001238919.1:n.-25-36del
NM_001251991.1:c.-25-36del	NP_001238920.1:n.-25-36del
NM_015895.4:c.-25-36del	NP_056979.1:n.-25-36del
XM_005249159.1:c.-25-36del	XP_005249216.1:n.-25-36del
XM_005249159.2:c.-25-36del	XP_005249216.1:n.-25-36del
NM_015895.5:c.-25-36del MANE Select	NP_056979.1:n.-25-36del
NM_001251989.2:c.-25-36del	NP_001238918.1:n.-25-36del
NM_001251990.2:c.-25-36del	NP_001238919.1:n.-25-36del