Canonical Allele Identifier: CA490206220

Gene: PATL2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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