Canonical Allele Identifier: CA7270092
Community Standard Title: NM_000428.3(LTBP2):c.804G>A (p.Pro268=)
Gene: LTBP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74585880C>T , CM000676.2:g.74585880C>T GRCh38
NC_000014.8:g.75052583C>T , CM000676.1:g.75052583C>T GRCh37
NC_000014.7:g.74122336C>T NCBI36
NG_021486.1:g.31452G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000428.3:c.804G>A MANE Select NP_000419.1:p.Pro268=
ENST00000261978.9:c.804G>A MANE Select ENSP00000261978.4:p.Pro268=
NM_000428.2:c.804G>A NP_000419.1:p.Pro268=
ENST00000261978.8:c.804G>A ENSP00000261978.4:p.Pro268=
ENST00000553939.5:c.804G>A ENSP00000452110.1:p.Pro268=
ENST00000556690.5:c.804G>A ENSP00000451477.1:p.Pro268=
ENST00000557425.1:n.123+26166G>A
XM_011536765.1:c.804G>A XP_011535067.1:p.Pro268=
XM_011536765.2:c.804G>A XP_011535067.1:p.Pro268=
XM_011536766.1:c.345G>A XP_011535068.1:p.Pro115=
XM_011536767.1:c.321G>A XP_011535069.1:p.Pro107=