Canonical Allele Identifier: CA490206798

Gene: PATL2

Linked Data

• MyVariant Identifiers: chr15:g.45003482G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711284G>C , CM000677.2:g.44711284G>C	GRCh38
NC_000015.9:g.45003482G>C , CM000677.1:g.45003482G>C	GRCh37
NC_000015.8:g.42790774G>C	NCBI36
NG_012920.1:g.4798G>C
NG_012920.2:g.4808G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-518C>G MANE Select	ENSP00000508024.1:n.-518C>G
ENST00000558573.1:n.33C>G
XM_011521338.1:c.-518C>G	XP_011519640.1:n.-518C>G
XM_011521339.1:c.-399C>G	XP_011519641.1:n.-399C>G
XM_011521340.1:c.-340C>G	XP_011519642.1:n.-340C>G
XM_011521343.1:c.-602C>G	XP_011519645.1:n.-602C>G
XM_011521345.1:c.-573C>G	XP_011519647.1:n.-573C>G
XM_011521338.3:c.-518C>G	XP_011519640.1:n.-518C>G
XM_011521339.3:c.-399C>G	XP_011519641.1:n.-399C>G
XM_011521340.3:c.-340C>G	XP_011519642.1:n.-340C>G
XM_011521343.3:c.-602C>G	XP_011519645.1:n.-602C>G
XM_011521345.3:c.-573C>G	XP_011519647.1:n.-573C>G
NM_001387260.1:c.-76+48C>G	NP_001374189.1:n.-76+48C>G
NM_001387261.1:c.-340C>G	NP_001374190.1:n.-340C>G
NM_001387262.1:c.-608C>G	NP_001374191.1:n.-608C>G
NM_001387263.1:c.-518C>G MANE Select	NP_001374192.1:n.-518C>G