Canonical Allele Identifier: CA37570171

Gene: PTPN14

Linked Data

• dbSNP Id: rs116573986
• gnomAD v3: 1-214501594-T-A
• gnomAD v4: 1-214501594-T-A
• MyVariant Identifiers: chr1:g.214674937T>A (hg19) ; chr1:g.214501594T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214501594T>A , CM000663.2:g.214501594T>A	GRCh38
NC_000001.10:g.214674937T>A , CM000663.1:g.214674937T>A	GRCh37
NC_000001.9:g.212741560T>A	NCBI36
NG_028036.1:g.55088A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366956.10:c.-154-36637A>T MANE Select	ENSP00000355923.4:n.-154-36637A>T
ENST00000366956.9:c.-154-36637A>T	ENSP00000355923.4:n.-154-36637A>T
ENST00000486173.1:n.232-36637A>T
ENST00000543945.5:c.-154-36637A>T	ENSP00000443330.1:n.-154-36637A>T
NM_005401.4:c.-154-36637A>T	NP_005392.2:n.-154-36637A>T
XR_247032.3:n.421-36637A>T
XM_017001941.1:c.-155+31723A>T	XP_016857430.1:n.-155+31723A>T
XM_024448759.1:c.-155+30870A>T	XP_024304527.1:n.-155+30870A>T
NM_005401.5:c.-154-36637A>T MANE Select	NP_005392.2:n.-154-36637A>T