Canonical Allele Identifier: CA3894171
Community Standard Title: NM_004370.6(COL12A1):c.1574A>T (p.Tyr525Phe)
Gene: COL12A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.75183367T>A , CM000668.2:g.75183367T>A GRCh38
NC_000006.11:g.75893083T>A , CM000668.1:g.75893083T>A GRCh37
NC_000006.10:g.75949803T>A NCBI36
NG_042181.1:g.27541A>T

Transcript Alleles

HGVS Amino-acid Change
NM_004370.6:c.1574A>T MANE Select NP_004361.3:p.Tyr525Phe
ENST00000322507.13:c.1574A>T MANE Select ENSP00000325146.8:p.Tyr525Phe
NM_004370.5:c.1574A>T NP_004361.3:p.Tyr525Phe
NM_080645.2:c.73+19353A>T NP_542376.2:n.73+19353A>T
NM_080645.3:c.73+19353A>T NP_542376.2:n.73+19353A>T
ENST00000322507.12:c.1574A>T ENSP00000325146.8:p.Tyr525Phe
ENST00000345356.10:c.73+19353A>T ENSP00000305147.9:n.73+19353A>T
ENST00000416123.6:c.1574A>T ENSP00000412864.2:p.Tyr525Phe
ENST00000483888.6:c.1574A>T ENSP00000421216.1:p.Tyr525Phe
ENST00000486533.1:n.680A>T
ENST00000615798.4:c.-1994A>T ENSP00000483232.1:n.-1994A>T
XM_011535434.1:c.1574A>T XP_011533736.1:p.Tyr525Phe
XM_011535435.1:c.1574A>T XP_011533737.1:p.Tyr525Phe
XM_011535436.1:c.73+19353A>T XP_011533738.1:n.73+19353A>T
XM_011535436.2:c.73+19353A>T XP_011533738.1:n.73+19353A>T
XM_017010252.2:c.1538A>T XP_016865741.1:p.Tyr513Phe