Canonical Allele Identifier: CA380369935

Gene: PTPRJ

Linked Data

• MyVariant Identifiers: chr11:g.48145194G>T (hg19) ; chr11:g.48123642G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123642G>T , CM000673.2:g.48123642G>T	GRCh38
NC_000011.9:g.48145194G>T , CM000673.1:g.48145194G>T	GRCh37
NC_000011.8:g.48101770G>T	NCBI36
NG_012209.1:g.148085G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.988G>T	ENSP00000514003.1:p.Ala330Ser
ENST00000418331.7:c.646G>T MANE Select	ENSP00000400010.2:p.Ala216Ser
ENST00000418331.6:c.646G>T	ENSP00000400010.2:p.Ala216Ser
ENST00000440289.6:c.646G>T	ENSP00000409733.2:p.Ala216Ser
ENST00000527952.1:c.382G>T	ENSP00000435618.1:p.Ala128Ser
ENST00000613246.4:c.646G>T	ENSP00000477933.1:p.Ala216Ser
ENST00000615445.4:c.646G>T	ENSP00000479342.1:p.Ala216Ser
NM_001098503.1:c.646G>T	NP_001091973.1:p.Ala216Ser
NM_002843.3:c.646G>T	NP_002834.3:p.Ala216Ser
XM_011520249.1:c.679G>T	XP_011518551.1:p.Ala227Ser
XR_930883.1:n.996G>T
XM_017018083.1:c.724G>T	XP_016873572.1:p.Ala242Ser
XM_017018084.1:c.667G>T	XP_016873573.1:p.Ala223Ser
XM_017018085.1:c.598G>T	XP_016873574.1:p.Ala200Ser
XR_930883.2:n.1055G>T
NM_002843.4:c.646G>T MANE Select	NP_002834.3:p.Ala216Ser
NM_001098503.2:c.646G>T	NP_001091973.1:p.Ala216Ser