Canonical Allele Identifier: CA490206222

Gene: PATL2

Linked Data

• MyVariant Identifiers: chr15:g.45003301A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711103A>G , CM000677.2:g.44711103A>G	GRCh38
NC_000015.9:g.45003301A>G , CM000677.1:g.45003301A>G	GRCh37
NC_000015.8:g.42790593A>G	NCBI36
NG_012920.1:g.4617A>G
NG_012920.2:g.4627A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-337T>C MANE Select	ENSP00000508024.1:n.-337T>C
ENST00000558573.1:n.214T>C
XM_011521338.1:c.-337T>C	XP_011519640.1:n.-337T>C
XM_011521339.1:c.-218T>C	XP_011519641.1:n.-218T>C
XM_011521340.1:c.-159T>C	XP_011519642.1:n.-159T>C
XM_011521343.1:c.-421T>C	XP_011519645.1:n.-421T>C
XM_011521345.1:c.-392T>C	XP_011519647.1:n.-392T>C
XM_011521338.3:c.-337T>C	XP_011519640.1:n.-337T>C
XM_011521339.3:c.-218T>C	XP_011519641.1:n.-218T>C
XM_011521340.3:c.-159T>C	XP_011519642.1:n.-159T>C
XM_011521343.3:c.-421T>C	XP_011519645.1:n.-421T>C
XM_011521345.3:c.-392T>C	XP_011519647.1:n.-392T>C
NM_001387260.1:c.-76+229T>C	NP_001374189.1:n.-76+229T>C
NM_001387261.1:c.-159T>C	NP_001374190.1:n.-159T>C
NM_001387262.1:c.-427T>C	NP_001374191.1:n.-427T>C
NM_001387263.1:c.-337T>C MANE Select	NP_001374192.1:n.-337T>C