Canonical Allele Identifier: CA390513667

Gene: POMT2

Linked Data

• gnomAD v4: 14-77278497-C-A
• MyVariant Identifiers: chr14:g.77744840C>A (hg19) ; chr14:g.77278497C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77278497C>A , CM000676.2:g.77278497C>A	GRCh38
NC_000014.8:g.77744840C>A , CM000676.1:g.77744840C>A	GRCh37
NC_000014.7:g.76814593C>A	NCBI36
NG_008897.1:g.47386G>T , LRG_844:g.47386G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555134.2:n.969G>T
ENST00000556394.2:c.1585G>T	ENSP00000451967.2:p.Asp529Tyr
ENST00000682247.1:c.2033G>T	ENSP00000507213.1:p.Gly678Val
ENST00000682395.1:n.2508G>T
ENST00000682459.1:n.1747G>T
ENST00000682467.1:c.1903G>T	ENSP00000508062.1:p.Asp635Tyr
ENST00000682795.1:c.2191G>T	ENSP00000507574.1:p.Asp731Tyr
ENST00000682895.1:n.1760G>T
ENST00000682955.1:n.1618G>T
ENST00000683188.1:c.2305G>T
ENST00000683380.1:n.1708G>T
ENST00000683907.1:c.309G>T	ENSP00000507754.1:n.309G>T
ENST00000684259.1:n.3811G>T
ENST00000684538.1:n.1423G>T
ENST00000684549.1:n.1595G>T
ENST00000261534.9:c.2044G>T MANE Select	ENSP00000261534.4:p.Asp682Tyr
ENST00000261534.8:c.2044G>T	ENSP00000261534.4:p.Asp682Tyr
ENST00000452340.7:n.3020G>T
ENST00000554767.5:n.2830G>T
ENST00000555710.1:c.405G>T	ENSP00000451730.1:n.405G>T
ENST00000556394.1:c.99G>T
ENST00000556446.1:n.345G>T
ENST00000602717.5:c.259G>T	ENSP00000487704.1:p.Asp87Tyr
NM_013382.5:c.2044G>T , LRG_844t1:c.2044G>T	NP_037514.2:p.Asp682Tyr
XM_011536675.1:c.2233G>T	XP_011534977.1:p.Asp745Tyr
XM_011536676.1:c.1900G>T	XP_011534978.1:p.Asp634Tyr
XM_011536677.1:c.1774G>T	XP_011534979.1:p.Asp592Tyr
XM_011536679.1:c.1327G>T	XP_011534981.1:p.Asp443Tyr
XR_943416.1:n.2297G>T
XM_011536675.2:c.2233G>T	XP_011534977.1:p.Asp745Tyr
XM_011536676.2:c.1900G>T	XP_011534978.1:p.Asp634Tyr
XM_011536677.3:c.1774G>T	XP_011534979.1:p.Asp592Tyr
XR_001750279.1:n.2330G>T
XR_001750282.1:n.2983G>T
XR_943416.3:n.2295G>T
NM_013382.6:c.2044G>T	NP_037514.2:p.Asp682Tyr
NM_013382.7:c.2044G>T MANE Select	NP_037514.2:p.Asp682Tyr