Canonical Allele Identifier: CA3892084

Gene: COL12A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75090126T>C , CM000668.2:g.75090126T>C	GRCh38
NC_000006.11:g.75799842T>C , CM000668.1:g.75799842T>C	GRCh37
NC_000006.10:g.75856562T>C	NCBI36
NG_042181.1:g.120782A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004370.6:c.8925A>G MANE Select	NP_004361.3:p.Gly2975=
ENST00000322507.13:c.8925A>G MANE Select	ENSP00000325146.8:p.Gly2975=
NM_004370.5:c.8925A>G	NP_004361.3:p.Gly2975=
NM_080645.2:c.5433A>G	NP_542376.2:p.Gly1811=
NM_080645.3:c.5433A>G	NP_542376.2:p.Gly1811=
ENST00000322507.12:c.8925A>G	ENSP00000325146.8:p.Gly2975=
ENST00000345356.10:c.5433A>G	ENSP00000305147.9:p.Gly1811=
ENST00000416123.6:c.8697A>G	ENSP00000412864.2:p.Gly2899=
ENST00000425443.6:c.1839A>G	ENSP00000399812.2:p.Gly613=
ENST00000483888.6:c.8913A>G	ENSP00000421216.1:p.Gly2971=
ENST00000511023.1:n.540A>G
ENST00000615798.4:c.5358A>G	ENSP00000483232.1:p.Gly1786=
ENST00000680981.1:n.334A>G
XM_011535434.1:c.8925A>G	XP_011533736.1:p.Gly2975=
XM_011535435.1:c.8652A>G	XP_011533737.1:p.Gly2884=
XM_011535436.1:c.5433A>G	XP_011533738.1:p.Gly1811=
XM_011535436.2:c.5433A>G	XP_011533738.1:p.Gly1811=
XM_017010252.2:c.8889A>G	XP_016865741.1:p.Gly2963=