Canonical Allele Identifier: CA10685569

Gene: TBX15

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.118961220C>G , CM000663.2:g.118961220C>G	GRCh38
NC_000001.10:g.119503843C>G , CM000663.1:g.119503843C>G	GRCh37
NC_000001.9:g.119305366C>G	NCBI36
NG_013361.1:g.33337G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369429.5:c.205+26371G>C MANE Select	ENSP00000358437.3:n.205+26371G>C
ENST00000207157.7:c.-114+28135G>C	ENSP00000207157.3:n.-114+28135G>C
ENST00000369429.3:c.205+26371G>C	ENSP00000358437.3:n.205+26371G>C
NM_152380.2:c.-114+28135G>C	NP_689593.2:n.-114+28135G>C
XM_005271161.2:c.205+26371G>C	XP_005271218.1:n.205+26371G>C
XM_005271162.1:c.205+26371G>C	XP_005271219.1:n.205+26371G>C
NM_001330677.1:c.205+26371G>C	NP_001317606.1:n.205+26371G>C
XM_005271161.4:c.205+26371G>C	XP_005271218.1:n.205+26371G>C
NM_001330677.2:c.205+26371G>C MANE Select	NP_001317606.1:n.205+26371G>C
NM_152380.3:c.-114+28135G>C	NP_689593.2:n.-114+28135G>C