Canonical Allele Identifier: CA3894124
Community Standard Title: NM_004370.6(COL12A1):c.1883A>G (p.Lys628Arg)
Gene: COL12A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.75183058T>C , CM000668.2:g.75183058T>C GRCh38
NC_000006.11:g.75892774T>C , CM000668.1:g.75892774T>C GRCh37
NC_000006.10:g.75949494T>C NCBI36
NG_042181.1:g.27850A>G

Transcript Alleles

HGVS Amino-acid Change
NM_004370.6:c.1883A>G MANE Select NP_004361.3:p.Lys628Arg
ENST00000322507.13:c.1883A>G MANE Select ENSP00000325146.8:p.Lys628Arg
NM_004370.5:c.1883A>G NP_004361.3:p.Lys628Arg
NM_080645.2:c.73+19662A>G NP_542376.2:n.73+19662A>G
NM_080645.3:c.73+19662A>G NP_542376.2:n.73+19662A>G
ENST00000322507.12:c.1883A>G ENSP00000325146.8:p.Lys628Arg
ENST00000345356.10:c.73+19662A>G ENSP00000305147.9:n.73+19662A>G
ENST00000416123.6:c.1883A>G ENSP00000412864.2:p.Lys628Arg
ENST00000483888.6:c.1883A>G ENSP00000421216.1:p.Lys628Arg
ENST00000486533.1:n.989A>G
ENST00000615798.4:c.-1685A>G ENSP00000483232.1:n.-1685A>G
XM_011535434.1:c.1883A>G XP_011533736.1:p.Lys628Arg
XM_011535435.1:c.1883A>G XP_011533737.1:p.Lys628Arg
XM_011535436.1:c.73+19662A>G XP_011533738.1:n.73+19662A>G
XM_011535436.2:c.73+19662A>G XP_011533738.1:n.73+19662A>G
XM_017010252.2:c.1847A>G XP_016865741.1:p.Lys616Arg