Canonical Allele Identifier: CA490206552

Gene: PATL2

Linked Data

• MyVariant Identifiers: chr15:g.45003398G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711200G>C , CM000677.2:g.44711200G>C	GRCh38
NC_000015.9:g.45003398G>C , CM000677.1:g.45003398G>C	GRCh37
NC_000015.8:g.42790690G>C	NCBI36
NG_012920.1:g.4714G>C
NG_012920.2:g.4724G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-434C>G MANE Select	ENSP00000508024.1:n.-434C>G
ENST00000558573.1:n.117C>G
XM_011521338.1:c.-434C>G	XP_011519640.1:n.-434C>G
XM_011521339.1:c.-315C>G	XP_011519641.1:n.-315C>G
XM_011521340.1:c.-256C>G	XP_011519642.1:n.-256C>G
XM_011521343.1:c.-518C>G	XP_011519645.1:n.-518C>G
XM_011521345.1:c.-489C>G	XP_011519647.1:n.-489C>G
XM_011521338.3:c.-434C>G	XP_011519640.1:n.-434C>G
XM_011521339.3:c.-315C>G	XP_011519641.1:n.-315C>G
XM_011521340.3:c.-256C>G	XP_011519642.1:n.-256C>G
XM_011521343.3:c.-518C>G	XP_011519645.1:n.-518C>G
XM_011521345.3:c.-489C>G	XP_011519647.1:n.-489C>G
NM_001387260.1:c.-76+132C>G	NP_001374189.1:n.-76+132C>G
NM_001387261.1:c.-256C>G	NP_001374190.1:n.-256C>G
NM_001387262.1:c.-524C>G	NP_001374191.1:n.-524C>G
NM_001387263.1:c.-434C>G MANE Select	NP_001374192.1:n.-434C>G