Canonical Allele Identifier: CA390382148

Gene: LTBP2

Linked Data

• MyVariant Identifiers: chr14:g.74967725A>T (hg19) ; chr14:g.74501022A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74501022A>T , CM000676.2:g.74501022A>T	GRCh38
NC_000014.8:g.74967725A>T , CM000676.1:g.74967725A>T	GRCh37
NC_000014.7:g.74037478A>T	NCBI36
NG_021486.1:g.116310T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261978.9:c.5328T>A MANE Select	ENSP00000261978.4:p.Asn1776Lys
ENST00000261978.8:c.5328T>A	ENSP00000261978.4:p.Asn1776Lys
ENST00000553939.5:c.*107T>A	ENSP00000452110.1:n.*107T>A
ENST00000554861.1:n.546T>A
ENST00000556690.5:c.5196T>A	ENSP00000451477.1:p.Asn1732Lys
NM_000428.2:c.5328T>A	NP_000419.1:p.Asn1776Lys
XM_011536765.1:c.4947T>A	XP_011535067.1:p.Asn1649Lys
XM_011536766.1:c.4869T>A	XP_011535068.1:p.Asn1623Lys
XM_011536767.1:c.4845T>A	XP_011535069.1:p.Asn1615Lys
XM_011536765.2:c.4947T>A	XP_011535067.1:p.Asn1649Lys
NM_000428.3:c.5328T>A MANE Select	NP_000419.1:p.Asn1776Lys