Canonical Allele Identifier: CA364744825
Community Standard Title: NM_004370.6(COL12A1):c.4300C>T (p.Arg1434Ter)
Gene: COL12A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.75147792G>A , CM000668.2:g.75147792G>A GRCh38
NC_000006.11:g.75857508G>A , CM000668.1:g.75857508G>A GRCh37
NC_000006.10:g.75914228G>A NCBI36
NG_042181.1:g.63116C>T

Transcript Alleles

HGVS Amino-acid Change
NM_004370.6:c.4300C>T MANE Select NP_004361.3:p.Arg1434Ter
ENST00000322507.13:c.4300C>T MANE Select ENSP00000325146.8:p.Arg1434Ter
NM_004370.5:c.4300C>T NP_004361.3:p.Arg1434Ter
NM_080645.2:c.808C>T NP_542376.2:p.Arg270Ter
NM_080645.3:c.808C>T NP_542376.2:p.Arg270Ter
ENST00000322507.12:c.4300C>T ENSP00000325146.8:p.Arg1434Ter
ENST00000345356.10:c.808C>T ENSP00000305147.9:p.Arg270Ter
ENST00000416123.6:c.4300C>T ENSP00000412864.2:p.Arg1434Ter
ENST00000419671.1:c.524C>T
ENST00000483888.6:c.4300C>T ENSP00000421216.1:p.Arg1434Ter
ENST00000615798.4:c.733C>T ENSP00000483232.1:p.Arg245Ter
XM_011535434.1:c.4300C>T XP_011533736.1:p.Arg1434Ter
XM_011535435.1:c.4027C>T XP_011533737.1:p.Arg1343Ter
XM_011535436.1:c.808C>T XP_011533738.1:p.Arg270Ter
XM_011535436.2:c.808C>T XP_011533738.1:p.Arg270Ter
XM_017010252.2:c.4264C>T XP_016865741.1:p.Arg1422Ter