Canonical Allele Identifier: CA14923996

Gene: LIF

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30242237T>G , CM000684.2:g.30242237T>G	GRCh38
NC_000022.10:g.30638226T>G , CM000684.1:g.30638226T>G	GRCh37
NC_000022.9:g.28968226T>G	NCBI36
NG_008721.1:g.9571A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249075.4:c.*1414A>C MANE Select	ENSP00000249075.3:n.*1414A>C
ENST00000249075.3:c.*1414A>C	ENSP00000249075.3:n.*1414A>C
NM_001257135.1:c.*1577A>C	NP_001244064.1:n.*1577A>C
NM_002309.4:c.*1414A>C	NP_002300.1:n.*1414A>C
XM_006724240.2:c.*1414A>C	XP_006724303.1:n.*1414A>C
XM_011530172.1:c.*1414A>C	XP_011528474.1:n.*1414A>C
XM_024452239.1:c.*1414A>C	XP_024308007.1:n.*1414A>C
XM_024452240.1:c.*1414A>C	XP_024308008.1:n.*1414A>C
NM_002309.5:c.*1414A>C MANE Select	NP_002300.1:n.*1414A>C
NM_001257135.2:c.*1577A>C	NP_001244064.1:n.*1577A>C