Canonical Allele Identifier: CA141000625
Community Standard Title: NM_004370.6(COL12A1):c.4616C>A (p.Thr1539Lys)
Gene: COL12A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.75145400G>T , CM000668.2:g.75145400G>T GRCh38
NC_000006.11:g.75855116G>T , CM000668.1:g.75855116G>T GRCh37
NC_000006.10:g.75911836G>T NCBI36
NG_042181.1:g.65508C>A

Transcript Alleles

HGVS Amino-acid Change
NM_004370.6:c.4616C>A MANE Select NP_004361.3:p.Thr1539Lys
ENST00000322507.13:c.4616C>A MANE Select ENSP00000325146.8:p.Thr1539Lys
NM_004370.5:c.4616C>A NP_004361.3:p.Thr1539Lys
NM_080645.2:c.1124C>A NP_542376.2:p.Thr375Lys
NM_080645.3:c.1124C>A NP_542376.2:p.Thr375Lys
ENST00000322507.12:c.4616C>A ENSP00000325146.8:p.Thr1539Lys
ENST00000345356.10:c.1124C>A ENSP00000305147.9:p.Thr375Lys
ENST00000416123.6:c.4616C>A ENSP00000412864.2:p.Thr1539Lys
ENST00000419671.1:c.840C>A
ENST00000474564.1:n.240C>A
ENST00000483888.6:c.4616C>A ENSP00000421216.1:p.Thr1539Lys
ENST00000615798.4:c.1049C>A ENSP00000483232.1:p.Thr350Lys
XM_011535434.1:c.4616C>A XP_011533736.1:p.Thr1539Lys
XM_011535435.1:c.4343C>A XP_011533737.1:p.Thr1448Lys
XM_011535436.1:c.1124C>A XP_011533738.1:p.Thr375Lys
XM_011535436.2:c.1124C>A XP_011533738.1:p.Thr375Lys
XM_017010252.2:c.4580C>A XP_016865741.1:p.Thr1527Lys