Canonical Allele Identifier: CA263607797
Community Standard Title: NM_000428.3(LTBP2):c.1199G>C (p.Cys400Ser)
Gene: LTBP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74552387C>G , CM000676.2:g.74552387C>G GRCh38
NC_000014.8:g.75019090C>G , CM000676.1:g.75019090C>G GRCh37
NC_000014.7:g.74088843C>G NCBI36
NG_021486.1:g.64945G>C

Transcript Alleles

HGVS Amino-acid Change
NM_000428.3:c.1199G>C MANE Select NP_000419.1:p.Cys400Ser
ENST00000261978.9:c.1199G>C MANE Select ENSP00000261978.4:p.Cys400Ser
NM_000428.2:c.1199G>C NP_000419.1:p.Cys400Ser
ENST00000261978.8:c.1199G>C ENSP00000261978.4:p.Cys400Ser
ENST00000553939.5:c.1199G>C ENSP00000452110.1:p.Cys400Ser
ENST00000556690.5:c.1199G>C ENSP00000451477.1:p.Cys400Ser
ENST00000557425.1:n.124-1037G>C
XM_011536765.1:c.1199G>C XP_011535067.1:p.Cys400Ser
XM_011536765.2:c.1199G>C XP_011535067.1:p.Cys400Ser
XM_011536766.1:c.740G>C XP_011535068.1:p.Cys247Ser
XM_011536767.1:c.716G>C XP_011535069.1:p.Cys239Ser