Canonical Allele Identifier: CA2625844100

Gene: POMT2

Linked Data

• gnomAD v4: 14-77286921-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77286926dup , CM000676.2:g.77286926dup	GRCh38
NC_000014.8:g.77753269dup , CM000676.1:g.77753269dup	GRCh37
NC_000014.7:g.76823022dup	NCBI36
NG_008897.1:g.38961dup , LRG_844:g.38961dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556394.2:c.795-100dup	ENSP00000451967.2:n.795-100dup
ENST00000682247.1:c.1254-100dup	ENSP00000507213.1:n.1254-100dup
ENST00000682382.1:c.826-100dup
ENST00000682395.1:n.1332dup
ENST00000682459.1:n.957-100dup
ENST00000682467.1:c.1254-100dup	ENSP00000508062.1:n.1254-100dup
ENST00000682706.1:n.30+61dup
ENST00000682795.1:c.1254-100dup	ENSP00000507574.1:n.1254-100dup
ENST00000682895.1:n.970-100dup
ENST00000682955.1:n.542-100dup
ENST00000683188.1:c.1129dup
ENST00000683328.1:c.247-100dup	ENSP00000508096.1:n.247-100dup
ENST00000683380.1:n.918-100dup
ENST00000683828.1:c.963-100dup
ENST00000684259.1:n.1105-100dup
ENST00000684549.1:n.805-100dup
ENST00000261534.9:c.1254-100dup MANE Select	ENSP00000261534.4:n.1254-100dup
ENST00000261534.8:c.1254-100dup	ENSP00000261534.4:n.1254-100dup
ENST00000452340.7:n.1277-100dup
ENST00000553880.5:n.125-100dup
ENST00000554767.5:n.2040-100dup
ENST00000554884.5:n.246-100dup
ENST00000556404.1:n.288dup
ENST00000556851.1:n.290-100dup
ENST00000557675.5:n.344-100dup
NM_013382.5:c.1254-100dup , LRG_844t1:c.1254-100dup	NP_037514.2:n.1254-100dup
XM_011536675.1:c.1254-100dup	XP_011534977.1:n.1254-100dup
XM_011536676.1:c.921-100dup	XP_011534978.1:n.921-100dup
XM_011536677.1:c.795-100dup	XP_011534979.1:n.795-100dup
XM_011536678.1:c.1254-100dup	XP_011534980.1:n.1254-100dup
XM_011536679.1:c.348-100dup	XP_011534981.1:n.348-100dup
XM_011536680.1:c.*307dup	XP_011534982.1:n.*307dup
XR_943416.1:n.1457-100dup
XM_011536675.2:c.1254-100dup	XP_011534977.1:n.1254-100dup
XM_011536676.2:c.921-100dup	XP_011534978.1:n.921-100dup
XM_011536677.3:c.795-100dup	XP_011534979.1:n.795-100dup
XR_001750279.1:n.1454-100dup
XR_001750282.1:n.1807dup
XR_943416.3:n.1455-100dup
NM_013382.6:c.1254-100dup	NP_037514.2:n.1254-100dup
NM_013382.7:c.1254-100dup MANE Select	NP_037514.2:n.1254-100dup