Canonical Allele Identifier: CA50045540

Gene: MEIS1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.66529844A>C , CM000664.2:g.66529844A>C	GRCh38
NC_000002.11:g.66756976A>C , CM000664.1:g.66756976A>C	GRCh37
NC_000002.10:g.66610480A>C	NCBI36
NG_011467.1:g.99445A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272369.14:c.888+17550A>C MANE Select	ENSP00000272369.8:n.888+17550A>C
ENST00000272369.13:c.888+17550A>C	ENSP00000272369.8:n.888+17550A>C
ENST00000398506.6:c.882+17550A>C	ENSP00000381518.2:n.882+17550A>C
ENST00000409517.5:n.203-18099A>C
ENST00000450027.2:n.343+17550A>C
ENST00000475239.5:n.448+17550A>C
ENST00000488550.5:c.888+17550A>C	ENSP00000475161.1:n.888+17550A>C
ENST00000495021.6:c.693+17550A>C	ENSP00000440571.1:n.693+17550A>C
ENST00000542964.5:n.321+17550A>C
ENST00000560281.6:c.888+17550A>C	ENSP00000454209.1:n.888+17550A>C
ENST00000606455.5:n.342+17550A>C
NM_002398.2:c.888+17550A>C	NP_002389.1:n.888+17550A>C
XM_005264321.1:c.936+17550A>C	XP_005264378.1:n.936+17550A>C
XM_005264322.1:c.888+17550A>C	XP_005264379.1:n.888+17550A>C
XM_005264323.1:c.936+17550A>C	XP_005264380.1:n.936+17550A>C
XM_005264324.3:c.693+17550A>C	XP_005264381.1:n.693+17550A>C
XM_005264325.3:c.693+17550A>C	XP_005264382.1:n.693+17550A>C
XR_244932.1:n.1523-18099A>C
XR_244933.1:n.1523-18099A>C
NM_002398.3:c.888+17550A>C MANE Select	NP_002389.1:n.888+17550A>C