Canonical Allele Identifier: CA13992055

Gene: FERMT2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.52886736A>G , CM000676.2:g.52886736A>G	GRCh38
NC_000014.8:g.53353454A>G , CM000676.1:g.53353454A>G	GRCh37
NC_000014.7:g.52423204A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341590.8:c.527-5267T>C MANE Select	ENSP00000340391.3:n.527-5267T>C
ENST00000341590.7:c.527-5267T>C	ENSP00000340391.3:n.527-5267T>C
ENST00000343279.8:c.527-5267T>C	ENSP00000342858.4:n.527-5267T>C
ENST00000395631.6:c.527-5267T>C	ENSP00000378993.2:n.527-5267T>C
ENST00000399304.7:c.527-5267T>C	ENSP00000382243.3:n.527-5267T>C
ENST00000553373.5:c.527-5267T>C	ENSP00000451084.1:n.527-5267T>C
ENST00000554152.5:c.353-4908T>C	ENSP00000450741.1:n.353-4908T>C
ENST00000554288.1:c.212-5267T>C	ENSP00000451268.1:n.212-5267T>C
ENST00000635305.1:c.42-4908T>C
NM_001134999.1:c.527-5267T>C	NP_001128471.1:n.527-5267T>C
NM_001135000.1:c.527-5267T>C	NP_001128472.1:n.527-5267T>C
NM_006832.2:c.527-5267T>C	NP_006823.1:n.527-5267T>C
XM_005267285.1:c.527-4908T>C	XP_005267342.1:n.527-4908T>C
XM_006720008.1:c.527-4908T>C	XP_006720071.1:n.527-4908T>C
XM_006720009.1:c.527-4908T>C	XP_006720072.1:n.527-4908T>C
XM_006720010.1:c.527-5267T>C	XP_006720073.1:n.527-5267T>C
XR_943867.1:n.525-11337A>G
XR_943868.1:n.399-11337A>G
XM_005267285.3:c.527-4908T>C	XP_005267342.1:n.527-4908T>C
XM_006720008.3:c.527-4908T>C	XP_006720071.1:n.527-4908T>C
XM_006720009.3:c.527-4908T>C	XP_006720072.1:n.527-4908T>C
XM_006720010.3:c.527-5267T>C	XP_006720073.1:n.527-5267T>C
XR_943867.2:n.551-11337A>G
NM_006832.3:c.527-5267T>C MANE Select	NP_006823.1:n.527-5267T>C
NM_001135000.2:c.527-5267T>C	NP_001128472.1:n.527-5267T>C
NM_001134999.2:c.527-5267T>C	NP_001128471.1:n.527-5267T>C