Canonical Allele Identifier: CA2594850949

Gene: COL11A2

Linked Data

• gnomAD v3: 6-33165108-T-G
• gnomAD v4: 6-33165108-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33165108T>G , CM000668.2:g.33165108T>G	GRCh38
NC_000006.11:g.33132885T>G , CM000668.1:g.33132885T>G	GRCh37
NC_000006.10:g.33240863T>G	NCBI36
NG_011589.1:g.32361A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.557-144A>C
ENST00000341947.7:c.4751-144A>C MANE Select	ENSP00000339915.2:n.4751-144A>C
ENST00000341947.6:c.4751-144A>C	ENSP00000339915.2:n.4751-144A>C
ENST00000361917.5:c.4430-144A>C	ENSP00000355123.1:n.4430-144A>C
ENST00000374708.8:c.4493-144A>C	ENSP00000363840.4:n.4493-144A>C
ENST00000477772.1:n.541-144A>C
NM_080679.2:c.4430-144A>C	NP_542410.2:n.4430-144A>C
NM_080680.2:c.4751-144A>C	NP_542411.2:n.4751-144A>C
NM_080681.2:c.4493-144A>C	NP_542412.2:n.4493-144A>C
XM_011514298.1:c.3905-144A>C	XP_011512600.1:n.3905-144A>C
XM_011514299.1:c.4037-144A>C	XP_011512601.1:n.4037-144A>C
XM_011514300.1:c.3857-144A>C	XP_011512602.1:n.3857-144A>C
XM_011514301.1:c.3794-144A>C	XP_011512603.1:n.3794-144A>C
XM_011514302.1:c.3638-144A>C	XP_011512604.1:n.3638-144A>C
XM_011514299.2:c.4037-144A>C	XP_011512601.1:n.4037-144A>C
XM_011514300.2:c.3857-144A>C	XP_011512602.1:n.3857-144A>C
XM_011514302.2:c.3638-144A>C	XP_011512604.1:n.3638-144A>C
XM_017010250.1:c.4751-144A>C	XP_016865739.1:n.4751-144A>C
XM_017010251.2:c.3569-144A>C	XP_016865740.1:n.3569-144A>C
NM_080680.3:c.4751-144A>C MANE Select	NP_542411.2:n.4751-144A>C
NM_080681.3:c.4493-144A>C	NP_542412.2:n.4493-144A>C
NM_080679.3:c.4430-144A>C	NP_542410.2:n.4430-144A>C