Canonical Allele Identifier: CA3892533
Community Standard Title: NM_004370.6(COL12A1):c.7541A>G (p.Asp2514Gly)
Gene: COL12A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.75116036T>C , CM000668.2:g.75116036T>C GRCh38
NC_000006.11:g.75825752T>C , CM000668.1:g.75825752T>C GRCh37
NC_000006.10:g.75882472T>C NCBI36
NG_042181.1:g.94872A>G

Transcript Alleles

HGVS Amino-acid Change
NM_004370.6:c.7541A>G MANE Select NP_004361.3:p.Asp2514Gly
ENST00000322507.13:c.7541A>G MANE Select ENSP00000325146.8:p.Asp2514Gly
NM_004370.5:c.7541A>G NP_004361.3:p.Asp2514Gly
NM_080645.2:c.4049A>G NP_542376.2:p.Asp1350Gly
NM_080645.3:c.4049A>G NP_542376.2:p.Asp1350Gly
ENST00000322507.12:c.7541A>G ENSP00000325146.8:p.Asp2514Gly
ENST00000345356.10:c.4049A>G ENSP00000305147.9:p.Asp1350Gly
ENST00000416123.6:c.7541A>G ENSP00000412864.2:p.Asp2514Gly
ENST00000425443.6:c.455A>G ENSP00000399812.2:p.Asp152Gly
ENST00000483888.6:c.7541A>G ENSP00000421216.1:p.Asp2514Gly
ENST00000493109.2:c.203A>G ENSP00000423423.1:p.Asp68Gly
ENST00000615798.4:c.3974A>G ENSP00000483232.1:p.Asp1325Gly
XM_011535434.1:c.7541A>G XP_011533736.1:p.Asp2514Gly
XM_011535435.1:c.7268A>G XP_011533737.1:p.Asp2423Gly
XM_011535436.1:c.4049A>G XP_011533738.1:p.Asp1350Gly
XM_011535436.2:c.4049A>G XP_011533738.1:p.Asp1350Gly
XM_017010252.2:c.7505A>G XP_016865741.1:p.Asp2502Gly