Canonical Allele Identifier: CA823317601

Gene: GMNN

Linked Data

• dbSNP Id: rs1444461900
• gnomAD v3: 6-24777117-AAAT-A
• gnomAD v4: 6-24777117-AAAT-A
• MyVariant Identifiers: chr6:g.24777346_24777348del (hg19) ; chr6:g.24777118_24777120del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24777122_24777124del , CM000668.2:g.24777122_24777124del	GRCh38
NC_000006.11:g.24777350_24777352del , CM000668.1:g.24777350_24777352del	GRCh37
NC_000006.10:g.24885329_24885331del	NCBI36
NG_030440.1:g.7192_7194del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230056.8:c.-25-100_-25-98del MANE Select	ENSP00000230056.3:n.-25-100_-25-98del
ENST00000230056.7:c.-25-100_-25-98del	ENSP00000230056.3:n.-25-100_-25-98del
ENST00000356509.7:c.-25-100_-25-98del	ENSP00000348902.3:n.-25-100_-25-98del
ENST00000378054.6:c.-25-100_-25-98del	ENSP00000367293.2:n.-25-100_-25-98del
ENST00000378059.3:c.-125_-123del	ENSP00000367298.3:n.-125_-123del
ENST00000468943.1:n.165-100_165-98del
ENST00000476555.5:c.-25-100_-25-98del	ENSP00000419584.1:n.-25-100_-25-98del
ENST00000620958.4:c.-25-100_-25-98del	ENSP00000477506.1:n.-25-100_-25-98del
NM_001251989.1:c.-25-100_-25-98del	NP_001238918.1:n.-25-100_-25-98del
NM_001251990.1:c.-25-100_-25-98del	NP_001238919.1:n.-25-100_-25-98del
NM_001251991.1:c.-25-100_-25-98del	NP_001238920.1:n.-25-100_-25-98del
NM_015895.4:c.-25-100_-25-98del	NP_056979.1:n.-25-100_-25-98del
XM_005249159.1:c.-25-100_-25-98del	XP_005249216.1:n.-25-100_-25-98del
XM_005249159.2:c.-25-100_-25-98del	XP_005249216.1:n.-25-100_-25-98del
NM_015895.5:c.-25-100_-25-98del MANE Select	NP_056979.1:n.-25-100_-25-98del
NM_001251989.2:c.-25-100_-25-98del	NP_001238918.1:n.-25-100_-25-98del
NM_001251990.2:c.-25-100_-25-98del	NP_001238919.1:n.-25-100_-25-98del