Canonical Allele Identifier: CA3894409

Gene: COL12A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75189695A>G , CM000668.2:g.75189695A>G	GRCh38
NC_000006.11:g.75899411A>G , CM000668.1:g.75899411A>G	GRCh37
NC_000006.10:g.75956131A>G	NCBI36
NG_042181.1:g.21213T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004370.6:c.515T>C MANE Select	NP_004361.3:p.Ile172Thr
ENST00000322507.13:c.515T>C MANE Select	ENSP00000325146.8:p.Ile172Thr
NM_004370.5:c.515T>C	NP_004361.3:p.Ile172Thr
NM_080645.2:c.73+13025T>C	NP_542376.2:n.73+13025T>C
NM_080645.3:c.73+13025T>C	NP_542376.2:n.73+13025T>C
ENST00000322507.12:c.515T>C	ENSP00000325146.8:p.Ile172Thr
ENST00000345356.10:c.73+13025T>C	ENSP00000305147.9:n.73+13025T>C
ENST00000416123.6:c.515T>C	ENSP00000412864.2:p.Ile172Thr
ENST00000483888.6:c.515T>C	ENSP00000421216.1:p.Ile172Thr
ENST00000615798.4:c.-3053T>C	ENSP00000483232.1:n.-3053T>C
XM_011535434.1:c.515T>C	XP_011533736.1:p.Ile172Thr
XM_011535435.1:c.515T>C	XP_011533737.1:p.Ile172Thr
XM_011535436.1:c.73+13025T>C	XP_011533738.1:n.73+13025T>C
XM_011535436.2:c.73+13025T>C	XP_011533738.1:n.73+13025T>C
XM_017010252.2:c.479T>C	XP_016865741.1:p.Ile160Thr