Canonical Allele Identifier: CA263841634

Gene: POMT2

Linked Data

• dbSNP Id: rs566361290
• gnomAD v2: 14-77772615-A-G
• gnomAD v3: 14-77306272-A-G
• gnomAD v4: 14-77306272-A-G
• MyVariant Identifiers: chr14:g.77772615A>G (hg19) ; chr14:g.77306272A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77306272A>G , CM000676.2:g.77306272A>G	GRCh38
NC_000014.8:g.77772615A>G , CM000676.1:g.77772615A>G	GRCh37
NC_000014.7:g.76842368A>G	NCBI36
NG_008897.1:g.19611T>C , LRG_844:g.19611T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000555675.6:n.232T>C
ENST00000556394.2:c.249-1472T>C	ENSP00000451967.2:n.249-1472T>C
ENST00000556880.6:n.436T>C
ENST00000682247.1:c.438+65T>C	ENSP00000507213.1:n.438+65T>C
ENST00000682382.1:c.386+65T>C
ENST00000682395.1:n.167+65T>C
ENST00000682459.1:n.102+130T>C
ENST00000682467.1:c.438+65T>C	ENSP00000508062.1:n.438+65T>C
ENST00000682795.1:c.438+65T>C	ENSP00000507574.1:n.438+65T>C
ENST00000682895.1:n.154+65T>C
ENST00000682955.1:n.102+130T>C
ENST00000683188.1:c.233+65T>C
ENST00000683380.1:n.102+130T>C
ENST00000683828.1:c.307+65T>C
ENST00000684102.1:n.249T>C
ENST00000684259.1:n.289+65T>C
ENST00000684479.1:n.105+65T>C
ENST00000684549.1:n.232T>C
ENST00000684600.1:c.252+65T>C
ENST00000684670.1:n.105+65T>C
ENST00000261534.9:c.438+65T>C MANE Select	ENSP00000261534.4:n.438+65T>C
ENST00000261534.8:c.438+65T>C	ENSP00000261534.4:n.438+65T>C
ENST00000452340.7:n.461+65T>C
ENST00000553863.5:n.102+130T>C
ENST00000554948.1:c.165+65T>C	ENSP00000452060.1:n.165+65T>C
ENST00000555675.5:n.154+65T>C
ENST00000555788.5:n.337T>C
ENST00000556326.5:c.*104+65T>C	ENSP00000450630.1:n.*104+65T>C
ENST00000556880.5:n.436T>C
ENST00000557525.1:n.528+65T>C
NM_013382.5:c.438+65T>C , LRG_844t1:c.438+65T>C	NP_037514.2:n.438+65T>C
XM_011536675.1:c.438+65T>C	XP_011534977.1:n.438+65T>C
XM_011536676.1:c.105+65T>C	XP_011534978.1:n.105+65T>C
XM_011536677.1:c.438+65T>C	XP_011534979.1:n.438+65T>C
XM_011536678.1:c.438+65T>C	XP_011534980.1:n.438+65T>C
XM_011536679.1:c.-226T>C	XP_011534981.1:n.-226T>C
XM_011536680.1:c.438+65T>C	XP_011534982.1:n.438+65T>C
XR_943416.1:n.641+65T>C
XM_011536675.2:c.438+65T>C	XP_011534977.1:n.438+65T>C
XM_011536676.2:c.105+65T>C	XP_011534978.1:n.105+65T>C
XM_011536677.3:c.438+65T>C	XP_011534979.1:n.438+65T>C
XR_001750279.1:n.638+65T>C
XR_001750282.1:n.642+65T>C
XR_943416.3:n.639+65T>C
NM_013382.6:c.438+65T>C	NP_037514.2:n.438+65T>C
NM_013382.7:c.438+65T>C MANE Select	NP_037514.2:n.438+65T>C