Canonical Allele Identifier: CA8494339

Gene: TMEM98

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.32931668G>C , CM000679.2:g.32931668G>C	GRCh38
NC_000017.10:g.31258686G>C , CM000679.1:g.31258686G>C	GRCh37
NC_000017.9:g.28282799G>C	NCBI36
NG_034264.1:g.8759G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_015544.3:c.131+9G>C MANE Select	NP_056359.2:n.131+9G>C
ENST00000579849.6:c.131+9G>C MANE Select	ENSP00000463245.1:n.131+9G>C
NM_001033504.1:c.131+9G>C	NP_001028676.1:n.131+9G>C
NM_001033504.2:c.131+9G>C	NP_001028676.1:n.131+9G>C
NM_001301746.1:c.131+9G>C	NP_001288675.1:n.131+9G>C
NM_001301746.2:c.131+9G>C	NP_001288675.1:n.131+9G>C
NM_015544.2:c.131+9G>C	NP_056359.2:n.131+9G>C
ENST00000261713.8:c.131+9G>C	ENSP00000261713.4:n.131+9G>C
ENST00000394642.7:c.131+9G>C	ENSP00000378138.3:n.131+9G>C
ENST00000395149.6:c.131+9G>C	ENSP00000398446.1:n.131+9G>C
ENST00000439138.5:c.131+9G>C	ENSP00000406394.1:n.131+9G>C
ENST00000578289.5:c.131+9G>C	ENSP00000464537.1:n.131+9G>C
ENST00000579849.5:c.131+9G>C	ENSP00000463245.1:n.131+9G>C
ENST00000582227.5:n.219+9G>C
ENST00000583120.1:n.201+9G>C
ENST00000583437.2:c.131+9G>C	ENSP00000463539.2:n.131+9G>C