Canonical Allele Identifier: CA2677549546

Gene: GMNN

Linked Data

• gnomAD v4: 6-24777226-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24777226C>T , CM000668.2:g.24777226C>T	GRCh38
NC_000006.11:g.24777454C>T , CM000668.1:g.24777454C>T	GRCh37
NC_000006.10:g.24885433C>T	NCBI36
NG_030440.1:g.7296C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230056.8:c.-21C>T MANE Select	ENSP00000230056.3:n.-21C>T
ENST00000230056.7:c.-21C>T	ENSP00000230056.3:n.-21C>T
ENST00000356509.7:c.-21C>T	ENSP00000348902.3:n.-21C>T
ENST00000378054.6:c.-21C>T	ENSP00000367293.2:n.-21C>T
ENST00000378059.3:c.-21C>T	ENSP00000367298.3:n.-21C>T
ENST00000468943.1:n.169C>T
ENST00000476555.5:c.-21C>T	ENSP00000419584.1:n.-21C>T
ENST00000620958.4:c.-21C>T	ENSP00000477506.1:n.-21C>T
NM_001251989.1:c.-21C>T	NP_001238918.1:n.-21C>T
NM_001251990.1:c.-21C>T	NP_001238919.1:n.-21C>T
NM_001251991.1:c.-21C>T	NP_001238920.1:n.-21C>T
NM_015895.4:c.-21C>T	NP_056979.1:n.-21C>T
XM_005249159.1:c.-21C>T	XP_005249216.1:n.-21C>T
XM_005249159.2:c.-21C>T	XP_005249216.1:n.-21C>T
NM_015895.5:c.-21C>T MANE Select	NP_056979.1:n.-21C>T
NM_001251989.2:c.-21C>T	NP_001238918.1:n.-21C>T
NM_001251990.2:c.-21C>T	NP_001238919.1:n.-21C>T