Canonical Allele Identifier: CA3894312

Gene: COL12A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75188437T>A , CM000668.2:g.75188437T>A	GRCh38
NC_000006.11:g.75898153T>A , CM000668.1:g.75898153T>A	GRCh37
NC_000006.10:g.75954873T>A	NCBI36
NG_042181.1:g.22471A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004370.6:c.922A>T MANE Select	NP_004361.3:p.Ile308Phe
ENST00000322507.13:c.922A>T MANE Select	ENSP00000325146.8:p.Ile308Phe
NM_004370.5:c.922A>T	NP_004361.3:p.Ile308Phe
NM_080645.2:c.73+14283A>T	NP_542376.2:n.73+14283A>T
NM_080645.3:c.73+14283A>T	NP_542376.2:n.73+14283A>T
ENST00000322507.12:c.922A>T	ENSP00000325146.8:p.Ile308Phe
ENST00000345356.10:c.73+14283A>T	ENSP00000305147.9:n.73+14283A>T
ENST00000416123.6:c.922A>T	ENSP00000412864.2:p.Ile308Phe
ENST00000483888.6:c.922A>T	ENSP00000421216.1:p.Ile308Phe
ENST00000486533.1:n.28A>T
ENST00000615798.4:c.-2646A>T	ENSP00000483232.1:n.-2646A>T
XM_011535434.1:c.922A>T	XP_011533736.1:p.Ile308Phe
XM_011535435.1:c.922A>T	XP_011533737.1:p.Ile308Phe
XM_011535436.1:c.73+14283A>T	XP_011533738.1:n.73+14283A>T
XM_011535436.2:c.73+14283A>T	XP_011533738.1:n.73+14283A>T
XM_017010252.2:c.886A>T	XP_016865741.1:p.Ile296Phe