Canonical Allele Identifier: CA2448039606

Gene: TNMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.100598283_100598284delinsTC , CM000685.2:g.100598283_100598284delinsTC	GRCh38
NC_000023.10:g.99853280_99853281delinsTC , CM000685.1:g.99853280_99853281delinsTC	GRCh37
NC_000023.9:g.99739936_99739937delinsTC	NCBI36
NG_013266.1:g.18491_18492delinsTC
NG_013266.2:g.18491_18492delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373031.5:c.577+626_577+627delinsTC MANE Select	ENSP00000362122.4:n.577+626_577+627delinsTC
ENST00000373031.4:c.577+626_577+627delinsTC	ENSP00000362122.4:n.577+626_577+627delinsTC
NM_022144.2:c.577+626_577+627delinsTC	NP_071427.2:n.577+626_577+627delinsTC
XM_005262175.3:c.388+626_388+627delinsTC	XP_005262232.1:n.388+626_388+627delinsTC
XM_005262176.1:c.577+626_577+627delinsTC	XP_005262233.1:n.577+626_577+627delinsTC
XM_011531008.1:c.388+626_388+627delinsTC	XP_011529310.1:n.388+626_388+627delinsTC
XM_011531009.1:c.388+626_388+627delinsTC	XP_011529311.1:n.388+626_388+627delinsTC
XM_011531010.1:c.388+626_388+627delinsTC	XP_011529312.1:n.388+626_388+627delinsTC
NM_022144.3:c.577+626_577+627delinsTC MANE Select	NP_071427.2:n.577+626_577+627delinsTC