Canonical Allele Identifier: CA2628213918

Gene: PATL2

Linked Data

• gnomAD v4: 15-44711136-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711141dup , CM000677.2:g.44711141dup	GRCh38
NC_000015.9:g.45003339dup , CM000677.1:g.45003339dup	GRCh37
NC_000015.8:g.42790631dup	NCBI36
NG_012920.1:g.4655dup
NG_012920.2:g.4665dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-371dup MANE Select	ENSP00000508024.1:n.-371dup
ENST00000558573.1:n.180dup
XM_011521338.1:c.-371dup	XP_011519640.1:n.-371dup
XM_011521339.1:c.-252dup	XP_011519641.1:n.-252dup
XM_011521340.1:c.-193dup	XP_011519642.1:n.-193dup
XM_011521343.1:c.-455dup	XP_011519645.1:n.-455dup
XM_011521345.1:c.-426dup	XP_011519647.1:n.-426dup
XM_011521338.3:c.-371dup	XP_011519640.1:n.-371dup
XM_011521339.3:c.-252dup	XP_011519641.1:n.-252dup
XM_011521340.3:c.-193dup	XP_011519642.1:n.-193dup
XM_011521343.3:c.-455dup	XP_011519645.1:n.-455dup
XM_011521345.3:c.-426dup	XP_011519647.1:n.-426dup
NM_001387260.1:c.-76+195dup	NP_001374189.1:n.-76+195dup
NM_001387261.1:c.-193dup	NP_001374190.1:n.-193dup
NM_001387262.1:c.-461dup	NP_001374191.1:n.-461dup
NM_001387263.1:c.-371dup MANE Select	NP_001374192.1:n.-371dup